iUUCD 2.0 - integrated annotations for ubiquitin and ubiquitin-like conjugation database

RNF212

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs151323310	snp	C/T	0.00517822	0.0506191	intron-variant	RNF212	GRCh38.p7	4:1103825	AAATTAGGAAAATGA[C/T]GAGGGCGCCAGCTAA	285498
rs180702838	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1110525	GCAAAACGGCAGAAA[A/C]TATGTTATGGTATGA	285498
rs180705656	snp	G/T	0.00636936	0.0560724	intron-variant	RNF212	GRCh38.p7	4:1103734	TTCAATACCATTCAT[G/T]ATGATTAAAAAAGAA	285498
rs180716834	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1084153	ATGAGGTTTCTCCAT[A/G]CTGGTCAGGTTGGTC	285498
rs180720807	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1065820	TGAAGTCCTGACCTC[A/G]AGTGATCTGTCCACT	285498
rs181013206	snp	C/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1091326	TTACAGGAGCCCCGG[C/G]TTCCATGCATGCTGT	285498
rs181029209	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1075967	GTGTCTGGCCACCTC[A/C]TAAGTTGAAGGAAGT	285498
rs181048302	snp	C/T	0.00119737	0.0244387	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	RNF212	GRCh38.p7	4:1056420	TTCAGGTGTCACTGC[C/T]CCAAGGTGAGCAGGT	285498
rs181102212	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1076925	GGTCTGCAAAGTCCA[A/C]ATGTTTTACTATCTG	285498
rs181106844	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1057425	AAATATGCAGCAGAC[A/G]GAGTGGGAGGCCACC	285498
rs181108431	snp	A/G	0.0023933	0.0345097	intron-variant	RNF212	GRCh38.p7	4:1103098	TTACAGACATGAAAA[A/G]TATGAGTGGATAACA	285498
rs181118113	snp	C/T	0.00358779	0.0422022	intron-variant	RNF212	GRCh38.p7	4:1083562	ACAATCGCTTGAACC[C/T]GGCAGGCGGAGGTTG	285498
rs181209252	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1064954	CAATGTTCATCCACG[C/T]GGTAGCGTGTGCCAG	285498
rs181248379	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1098165	CCTCCTCCCATTCTG[C/T]GGTTCAGGACAGTGA	285498
rs181251430	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1080171	GACAGGAAAACATCA[C/T]AGGATTCATTTTGCG	285498
rs181268792	snp	C/G			intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1093039	GGTAGGGCAGAGGCT[C/G]GGTGGATGGAACGGA	285498
rs181336162	snp	C/G/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1111513	TCTCCAGTGTTTTGT[C/G/T]TAGCAGTGAAACCCT	285498
rs181337323	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1107272	TAGCCAGGATGGTCT[C/T]GATCTCCTGACCTCA	285498
rs181353714	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1069954	GTACAGCTGTGTCAG[C/T]GTGGACGCCTAGCCT	285498
rs181400996	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1097707	ACTTTCCCCAGCCAG[A/G]ACCACATTAGCACAA	285498
rs181469061	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1061657	AGAGCAGCGGCCAAC[C/T]GCTGAGCTGTAAAGA	285498
rs181477324	snp	A/G	0.00159617	0.0282053	intron-variant	RNF212	GRCh38.p7	4:1087474	TGGGTGGGGGTGACA[A/G]GATGGGGTGAGGGTG	285498
rs181488265	snp	A/G	0.0244538	0.107838	intron-variant	RNF212	GRCh38.p7	4:1088121	TGGAGGGCTCAGAAA[A/G]AGACAGAAAGGTGTG	285498
rs181616121	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1107840	AAAAAAACAACTATT[A/G]TATTTAAATCATCAG	285498
rs181630663	snp	A/G	0.00517822	0.0506191	downstream-variant-500B, intron-variant	RNF212	GRCh38.p7	4:1071288	CTTGGTTTTTAAAAT[A/G]CTATTCTTACAATTT	285498
rs181665370	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1061404	GAGGGGTAAGGAGGG[A/C]AGGGACCAGTCAGAA	285498
rs181841120	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1087799	TTCTCACGAGATCTG[A/C]TGGTTTAAAAGTGTT	285498
rs181854830	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1070556	CGCCTGGCCTGAGTT[A/G]CAGGTGGTTTTGTAG	285498
rs181922718	snp	A/G	0.00318978	0.0398085	intron-variant	RNF212	GRCh38.p7	4:1107686	TGATCTCCTGATCTC[A/G]TGATCCGCCCATCTT	285498
rs182031869	snp	C/T	0.00874735	0.0655527	intron-variant	RNF212	GRCh38.p7	4:1060891	GGGTCCAGGACCTGC[C/T]GTTCAACAACTCATT	285498
rs182050138	snp	A/G	0.000399281	0.0141238	intron-variant, missense, downstream-variant-500B	RNF212	GRCh38.p7	4:1093767	GGGGACTTGGTGTGA[A/G]TGAGGGTCCTGCTGG	285498
rs182059192	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1077152	AGAATTCCTTGAACC[C/T]GGGAGGCGGAGGTTG	285498
rs182064796	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1057859	CACCTGAGGTCGGGA[A/G]TTCGAGACCAGCCTG	285498
rs182187718	snp	A/C/T	0.0023933	0.0345097	intron-variant	RNF212	GRCh38.p7	4:1110975	CCAGTCACCTGCCAA[A/C/T]GCAGAGTATGCTGAC	285498
rs182309573	snp	A/G	0.0944967	0.195752	intron-variant	RNF212	GRCh38.p7	4:1079023	CACAGGGTCAACACA[A/G]GACCAACATGGGACC	285498
rs182460871	snp	C/T	0.00199481	0.0315187	intron-variant	RNF212	GRCh38.p7	4:1092778	CACGCGTGCTTTGCC[C/T]GCATCCTGCGAACTG	285498
rs182573166	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF212	GRCh38.p7	4:1071950	TGAAAACATGTCTAC[A/G]CAAAACCCTGGCACA	285498
rs182650417	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1104842	CTGACATCTAATGGC[A/G]GCACGGGGCAGGACA	285498
rs182709108	snp	C/G/T	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1105198	GGCTACTCCTTTCCA[C/G/T]GTGTGTGTGTAAAAA	285498
rs182748278	snp	A/G/T			intron-variant	RNF212	GRCh38.p7	4:1087123	GTGAGAGGACGGGGT[A/G/T]GGGGAGAGAGGATGG	285498
rs182788198	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1101402	TTTTCAAGTGGTCAA[A/G]CTCTGGCTCATCGTT	285498
rs182860860	snp	C/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1081360	GGTTGGGATGGGAAG[C/G]CAGGTGCAGAATCGG	285498
rs182866979	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1062045	AAATATGATGATAGT[A/G]ACTCCAGGCACAGGG	285498
rs182941428	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1100152	CTTTTGCTTGCTGCC[C/T]GTGTGGACTTTGCAC	285498
rs182984371	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1067418	TAGATTATAATAGAT[C/T]AAAAAAAGATCTAAC	285498
rs183132878	snp	A/C	0.00183351	0.0302224	intron-variant	RNF212	GRCh38.p7	4:1081653	GGTATTGAATTAAAT[A/C]ATAAAAACTGACTTC	285498
rs183135685	snp	C/T	0.0023933	0.0345097	intron-variant	RNF212	GRCh38.p7	4:1108764	CTGCAAGTGGCATGA[C/T]CACAGCTCACTGCAG	285498
rs183167944	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1096655	GCTCCATGGTCTCGG[A/G]ATAGTGCACCTGGCT	285498
rs183192930	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1109511	CCTCTGGGCCAGTGC[A/G]GCTAAGAACTAGGAA	285498
rs183208944	snp	G/T	0.00318978	0.0398085	intron-variant	RNF212	GRCh38.p7	4:1089079	GAGAAGCCATGAGAA[G/T]AGGGCCACTGTCCTC	285498
rs183214373	snp	A/C	0.000798403	0.0199641	utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1072707	ATTGTCTCTAAAATT[A/C]AAAGGTCAAATATAA	285498
rs183254893	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1085996	TATCAGACAGGCTAT[A/G]CTGAGTGACATGTGA	285498
rs183404448	snp	C/T	0.00199481	0.0315187	intron-variant	RNF212	GRCh38.p7	4:1062694	AGTCCTGCAGTGGGA[C/T]GGGAAGTGAAAAGAT	285498
rs183416874	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1088514	AAAGTCTGAACAAAA[C/T]TGCAGCGCGACCATG	285498
rs183417554	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1085725	TGTCTCCCTTCTTCC[C/G]TTCGGTTTTCCCACA	285498
rs183447603	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1066447	AATTCGCCCACTTCA[A/G]CTTCCTGAGCAGCCG	285498
rs183670486	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF212, LOC105374344	GRCh38.p7	4:1114563	TATATTAGGTTAAAT[A/G]TATATCAGTAGCGTT	285498
rs183671363	snp	A/T	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1096680	CTGGCTCATCACAGA[A/T]CCAAGCACACCCCTC	285498
rs183677040	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1078801	AACACAGGACCGACA[C/T]GGGACCAACACAGGG	285498
rs183786127	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1110890	GCACTCAGACTACTG[C/G]AATCTGTGTTGACCT	285498
rs183792524	snp	C/G	0.00279162	0.0372561	intron-variant	RNF212	GRCh38.p7	4:1092452	TACACCAGCCTCCAG[C/G]ACTCCATTAGGGGGA	285498
rs183824160	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1076051	AGATATGTTAATCCT[G/T]GTCAATTTTACATAA	285498
rs183841757	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1099024	CACCCCAGGATGTCC[A/T]GAAGATGAGCCTAGA	285498
rs183874407	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1061732	GAAACCATGAGCGGA[C/T]ACATCTGCGGCTGCC	285498
rs184038023	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1080628	ATTAAAACTCCTCAC[A/G]GGAAACCTGCCTGGA	285498
rs184043580	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1077662	GCTGTGAGTTCATCC[A/G]TGAAACAAGGCCCTA	285498
rs184138911	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1078236	AACACAGGCATTCAC[C/T]GCCGCCAGAACACAC	285498
rs184143819	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1059021	AAAGGGGAGATGTGA[C/T]GACTGAGTTCTCAAG	285498
rs184166450	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1087723	TGTCAAGGGGAAGAA[C/T]CTGGGGGAGGTGATT	285498
rs184182494	snp	A/C	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1095188	GTCTCGGGATAGCGC[A/C]CCTGGCTCATCACAG	285498
rs184195197	snp	A/C			intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1058204	AGCAGTTTTATTTTG[A/C]TGACAATTTCCTTTA	285498
rs184201033	snp	C/T	0.0185938	0.0946107	intron-variant	RNF212	GRCh38.p7	4:1060568	TAACCATTCCCACAA[C/T]ATCTTCCAGCGCAGC	285498
rs184214587	snp	A/C	0.0271762	0.113356	intron-variant	RNF212	GRCh38.p7	4:1102833	CTCCAGCCTAGGCAA[A/C]AGAGCGAGACTCCGT	285498
rs184230819	snp	A/G/T	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1063572	CAGGTGTGGTGGTGC[A/G/T]CACCTGTAATCCCAG	285498
rs184268242	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1090616	TTGGGCAAATAGGCT[A/G]CTCAGAAGGAGACAG	285498
rs184277638	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1074974	TCCCCTTGACATCAC[C/T]GTCCCTTCGAACTAC	285498
rs184283280	snp	C/G	0.000399281	0.0141238	downstream-variant-500B	RNF212	GRCh38.p7	4:1056028	GGCCCGCTGTGAGTA[C/G]TGTGTGACCAGAATG	285498
rs184390351	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1102225	AATATAAAATGGACA[C/T]GATCAACAGAGCTAA	285498
rs184417719	snp	C/T	0.00159617	0.0282053	intron-variant	RNF212	GRCh38.p7	4:1107293	CCTGACCTCATGATC[C/T]GCCTGCCTCAGCCTC	285498
rs184516710	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	RNF212	GRCh38.p7	4:1056459	AGGCATGGAAGTCGC[A/G]GTAAAAACACAACTT	285498
rs184522492	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1082437	ACATGAGGGGTGGGG[C/T]TGTCTCCTGGCACCG	285498
rs184798736	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1106750	GGTACCGTGCGAGGA[A/G]CAGAAGCAGGCAGGC	285498
rs184801767	snp	A/T			intron-variant	RNF212	GRCh38.p7	4:1087147	AGGATGGGGTGGGGG[A/T]GAGAGGATGGGTGGG	285498
rs184811680	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1068896	AGCAGAAAATACAAA[C/T]CTCTGAACAAAATAG	285498
rs184972815	snp	G/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1110178	AAAGACAAAGGGATT[G/T]ATGCCTGATCTATAA	285498
rs185016457	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1098578	TGTAACACCCTCCTA[C/T]ACACACCAAACTGCA	285498
rs185059352	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1089309	TTTAAGATTTAATGG[C/G]TGCCCTGCTGGGTTC	285498
rs185161924	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1110054	TATGCACCATCACAG[A/C]TAGGAGTCATGCAGT	285498
rs185173974	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1073825	TCTGTGTTCACCTCC[C/T]GACTCTGCCTGCTGG	285498
rs185178151	snp	C/G	0.00199481	0.0315187	intron-variant	RNF212	GRCh38.p7	4:1069958	AGCTGTGTCAGCGTG[C/G]ACGCCTAGCCTGAAT	285498
rs185200823	snp	C/G	0.00159617	0.0282053	intron-variant	RNF212	GRCh38.p7	4:1107078	TTTTTTTTAGACTGA[C/G]TCTTGCTCTGTCGCC	285498
rs185214597	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1069131	CACAAGAATCGCTTG[A/T]ACCTGGGAGGCAGAG	285498
rs185318226	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1087252	TAGGGGAGAGAGGAC[A/G]GGGTAGGGGAGAGAG	285498
rs185328923	snp	A/G	0.00199481	0.0315187	intron-variant	RNF212	GRCh38.p7	4:1065994	CAATCCTGCCTCTGT[A/G]TTCCAAGTAGCTAGG	285498
rs185511741	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1063391	ACCTACAGGACAATA[C/T]GATTAACAGCTGACT	285498
rs185621175	snp	C/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1111531	GCAGTGAAACCCTGT[C/G]CAGTTCTCTAGCCCT	285498
rs185637325	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1093227	AGTTTTGCACTCTTA[A/G]AAGTTACTGAGGGCC	285498
rs185641321	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1076998	ACTTTGGGACGCTGA[A/G]GTGGGCAGATCACAA	285498
rs185650284	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1057567	ACCCATTAATTTACA[C/T]ACTGCCTGCCCCGGC	285498
rs185739052	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB, nc-transcript-variant, intron-variant	RNF212, TMED11P, LOC105374344	GRCh38.p7	4:1115316	TCATTTGGAAAATTC[C/T]GACTGAGATAAAGAT	285498
rs185796710	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1060952	CTACAGTGGAGTAGA[A/G]ATCAATGAGTTATCT	285498
rs185805823	snp	A/G	0.00755907	0.0610114	intron-variant	RNF212	GRCh38.p7	4:1061678	GCTGTAAAGACAGGC[A/G]GACACCCCGGGACAT	285498
rs185883065	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1097802	AAGAAAAGAGGCTCA[C/T]GCCTGTCATCCCAGC	285498
rs185885173	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1079914	CTCCAGGACAGAGGC[C/T]GCTGGCCGGCCCGCC	285498
rs185897511	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1061483	CCCTGGAACCCTGGC[C/T]GACAGAAGCAGCACA	285498
rs185960021	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1103756	AAAAAAGAAACCTTA[A/G]CAAAAACTTGATGCA	285498
rs186021091	snp	C/T	0.00557542	0.0525036	intron-variant	RNF212	GRCh38.p7	4:1104471	GGCAGTGGAGGGCTG[C/T]CCAGGAGGCTGTTTT	285498
rs186026441	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1085729	TCCCTTCTTCCCTTC[A/G]GTTTTCCCACAGCAT	285498
rs186027188	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1080194	ATTTTGCGTTGGCCC[C/T]CTCCTAGCCCTGCCA	285498
rs186034930	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1066769	TTTACTCTATTGATA[A/G]TATCTTTTGATGTGG	285498
rs186091888	snp	C/T	0.00318978	0.0398085	intron-variant	RNF212	GRCh38.p7	4:1084359	AGGAGGCTTTGCTGT[C/T]CACATAAGGTCTCCG	285498
rs186396417	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1078923	ACACAGGACCAACAC[A/G]GGACCAACACAGGGT	285498
rs186528408	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1083911	AATTATACACCAACA[A/C]GGAAAAAAATGAAAG	285498
rs186564835	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1107748	AGCCATCACGCCCGG[C/G]AGGACTTACACATTT	285498
rs186581731	snp	C/T	0.00159617	0.0282053	intron-variant	RNF212	GRCh38.p7	4:1087835	GTTCCCCTCCACCCC[C/T]TCTCCTGCCGCTATG	285498
rs186582413	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1088815	CAATTTGGGCTGCTG[C/G]TTCAGAGGGAGCAAA	285498
rs186589061	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1070778	CACCACATCGGTAAC[A/G]TGCTCAGTGGTTCAG	285498
rs186598604	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF212	GRCh38.p7	4:1072369	CCCATAGAACATTCG[A/T]CACCTAGAGTGAACC	285498
rs186598993	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1057078	AGTTACAGCACTGGC[C/T]GTTTTGTGGTTTTAA	285498
rs186697542	snp	C/T	0.00279162	0.0372561	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1092826	GAGAGTCAAGGCAGT[C/T]GGGGGAGAATGCAGG	285498
rs186715978	snp	A/T			intron-variant	RNF212	GRCh38.p7	4:1087090	GGACAGGAGTGGGGG[A/T]GAGAGGACGGGGTGG	285498
rs186722301	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1068049	CAATTCTCCCCACAC[C/T]GATGTAGAGATTCAA	285498
rs186724715	snp	A/C	0.00279162	0.0372561	intron-variant	RNF212	GRCh38.p7	4:1094849	AGGACCCCAGAACTG[A/C]CTGAGACCACTTTGT	285498
rs186740173	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1103580	GTTCCTAGAATCTAA[C/T]GTGGGTTTCAAATTC	285498
rs186761330	snp	A/G/T	0.0237078	0.106494	downstream-variant-500B, intron-variant	RNF212	GRCh38.p7	4:1071300	AATACTATTCTTACA[A/G/T]TTTTTTCTGTGTGCT	285498
rs186763482	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1065112	TCTTGGGTATACAAG[C/T]ATCTCTTAGAGACCC	285498
rs186831303	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1076536	GCTCTCTGCAGGCCA[A/G]AGAGTGAGACCTCAG	285498
rs186863067	snp	C/T	0.000149025	0.00863078	intron-variant	RNF212	GRCh38.p7	4:1108325	ATTAAGATGCAGATA[C/T]GACACATTTCAACTT	285498
rs186897279	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1111050	CACCACGAAGGCACA[C/T]GCGTCTCCATCATTC	285498
rs186994589	snp	G/T	0.0221141	0.102801	upstream-variant-2KB, intron-variant	RNF212, LOC105374344	GRCh38.p7	4:1114365	GACGCTGCAAAGCTC[G/T]GATCGAGAGGCTCAG	285498
rs187007397	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1078721	ACCAGCACGGGACCA[A/G]CATGGGACCAGCAGA	285498
rs187023071	snp	A/G	0.00199481	0.0315187	intron-variant	RNF212	GRCh38.p7	4:1059235	TCTTGTCTTTGCCCC[A/G]GGGCTGTGCAGACCT	285498
rs187348188	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1106886	TTATGCCACAGAAAT[A/G]TTCTTATAAGTGTGG	285498
rs187382699	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1080814	CTATCACAGGGGTGG[A/G]CTGAATTTGTGCCTT	285498
rs187527868	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1063032	CACTGAAAACTGCAA[A/G]ATACCGTTGAAAGAA	285498
rs187559388	snp	A/T	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1109570	TCACAGACTTGAGGA[A/T]TCCAACGCTGCTGAG	285498
rs187569047	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1089241	GGCCTTGGGAGCCCC[C/G]CTACCCTTAAATCAG	285498
rs187572097	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1072801	CAAAGGAATAAAGCA[G/T]ATAATTTGTAGAAAA	285498
rs187578126	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1100236	GTCTTGTTTTGTGTT[C/T]CTGTCAAACATTCTG	285498
rs187586767	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1101774	GCTCTTCCTTCTCAG[C/T]GCAAAAATATCTGTA	285498
rs187589316	snp	C/T	0.000428915	0.0146381	intron-variant	RNF212	GRCh38.p7	4:1081397	CTGCAGGTCCTGTGA[C/T]TTCTGCAAGCAACCC	285498
rs187593744	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1062078	TTCAACACAAAAACA[A/G]AAATGCTAAAGAAAA	285498
rs187633376	snp	A/G	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1099149	CCATTCCTCCACCCC[A/G]GCACTCACATTGCAG	285498
rs187646399	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1105392	ACCACCCAACCAATA[C/T]GGTGGTGCCCTATTC	285498
rs187653233	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1061877	CCCAGGTTGTCCAGA[C/T]TGCAGCCCCAAATTA	285498
rs187677053	snp	C/T	0.00159617	0.0282053	intron-variant	RNF212	GRCh38.p7	4:1077159	CTTGAACCCGGGAGG[C/T]GGAGGTTGCAGTGAG	285498
rs187688273	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1095180	GCTCCATGGTCTCGG[A/G]ATAGCGCACCTGGCT	285498
rs187777870	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1108838	CTGAGTAGCTAGGAC[A/C]ACAGACGTGTGCCGC	285498
rs187830885	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1086335	GTCAGGCTGGAGCCC[A/C]GCCCTGTGTGTGGGA	285498
rs187867500	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1057862	CTGAGGTCGGGAGTT[C/T]GAGACCAGCCTGACC	285498
rs188102146	snp	A/C	0.00557542	0.0525036	intron-variant	RNF212	GRCh38.p7	4:1104935	ATTTGAGGATGGGTG[A/C]TGGGGGCTCCTCCCC	285498
rs188260808	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1110413	TTGGGTCGCATTTGG[A/G]TCAGTTTTCATGTGC	285498
rs188267110	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1091120	AATCACAGGGTGCTG[A/T]CCCTCTGATAATGGC	285498
rs188271143	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1075270	TCACATTTAACTGGT[A/G]TATTAGGCCATTCTT	285498
rs188282703	snp	A/G	0.000798403	0.0199641	downstream-variant-500B	RNF212	GRCh38.p7	4:1056061	TAGTAATCACCTAAC[A/G]CAGGATGTGGCGGCG	285498
rs188299565	snp	C/T	0.00953873	0.0683987	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1058307	TGAAGAAGGTGCTTG[C/T]GGGGGGGCACTACCT	285498
rs188405211	snp	C/T	0.0279526	0.114869	intron-variant	RNF212	GRCh38.p7	4:1107508	TCACCCAGGCTGGAG[C/T]GCAGTGGCGCCATCT	285498
rs188409220	snp	A/G	0.00716266	0.059414	intron-variant	RNF212	GRCh38.p7	4:1087791	ACAGTGAGTTCTCAC[A/G]AGATCTGATGGTTTA	285498
rs188414164	snp	C/T	0.00358779	0.0422022	upstream-variant-2KB, intron-variant	RNF212, LOC105374344	GRCh38.p7	4:1114575	AATATATATCAGTAG[C/T]GTTGATTTTACCCTT	285498
rs188421145	snp	C/T	0.00874735	0.0655527	intron-variant	RNF212	GRCh38.p7	4:1070292	GCCTGGCCTGAGTTA[C/T]GGGTGGTTTTGTAGG	285498
rs188432437	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1097979	CTGAGGCAGAAGAAT[C/T]GCTTGAACCCGGGAG	285498
rs188443969	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1074488	AATCCACAGGCCCTT[C/T]CAGTACACCGTGGAA	285498
rs188444617	snp	A/C	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1080097	TCACTCACTGCCTGG[A/C]CACACATACCACACC	285498
rs188520434	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1110153	ACAGAGAGGAAATCA[C/T]GTGCGGCCAAAAGAC	285498
rs188575951	snp	A/C	0.00398564	0.0444627	intron-variant	RNF212	GRCh38.p7	4:1077797	CAGGGCCTGAGGGGG[A/C]AGGTGGGGTCCTCGA	285498
rs188658198	snp	A/C/G	0.000802545	0.020016	missense, upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant	RNF212, LOC105374344	GRCh38.p7	4:1113361	AAGCCCTGACCTTTG[A/C/G]CGAGGCAGGCGTCGC	285498
rs188719696	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1089483	AACTTGCCTTGTCTC[C/T]GATGAGATTTTGGGC	285498
rs188922380	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1061305	GCTTCCAGAGGGGGT[A/G]GGCTCAAGGTGGGAG	285498
rs188929651	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1087238	GAGAGAGGACGGGGT[A/G]GGGGAGAGAGGACGG	285498
rs188933694	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1068926	GAAATCTATGAATAT[G/T]GCTGGACGCAATGGC	285498
rs188988195	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1063637	ACCCAGAGGTGGAGG[C/T]TGCAGTGAGATCACA	285498
rs189075001	snp	G/T	0.0023933	0.0345097	intron-variant	RNF212	GRCh38.p7	4:1083353	GGACAGAACAAAAAC[G/T]CAATGGGGGCCGGGT	285498
rs189122922	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1103603	TCAAATTCTAAAAAT[A/G]AATGCAACTCACCAC	285498
rs189143145	snp	G/T	0.00676609	0.0577691	intron-variant	RNF212	GRCh38.p7	4:1065656	TAGAGAGGGGGTTTT[G/T]CCCAGGCTGGTCTGG	285498
rs189162173	snp	A/G	0.00517822	0.0506191	intron-variant	RNF212	GRCh38.p7	4:1063570	GCCAGGTGTGGTGGT[A/G]CGCACCTGTAATCCC	285498
rs189359669	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1110934	CTAGGCAAACCTGTG[A/T]ATCTATACCTGCCCC	285498
rs189379725	snp	A/G/T			intron-variant	RNF212	GRCh38.p7	4:1087257	GAGAGAGGACGGGGT[A/G/T]GGGGAGAGAGGATGG	285498
rs189416418	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1084026	TGATCTTGGCTCACC[A/G]CAACCTCTGCCTCCC	285498
rs189519849	snp	C/T	0.00279162	0.0372561	intron-variant	RNF212	GRCh38.p7	4:1060779	AGAGTGAGCGCCCTG[C/T]GCCCCTGCTGACAGG	285498
rs189658513	snp	A/G	0.0197687	0.0974348	intron-variant	RNF212	GRCh38.p7	4:1107091	GAGTCTTGCTCTGTC[A/G]CCCAGGCTGGAGTGC	285498
rs189670789	snp	G/T	0.021333	0.101051	intron-variant	RNF212	GRCh38.p7	4:1057789	CAAACTCCTGGCTGG[G/T]CATGGTGGCTCACGC	285498
rs189898483	snp	G/T	0.00279162	0.0372561	intron-variant	RNF212	GRCh38.p7	4:1108893	TTTTGTAGAGACAGG[G/T]TCTCACTATGTTGCC	285498
rs189900297	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1089034	TGCGGTGGTTGTTCC[C/T]ACACAGTGTCCCAAC	285498
rs189909552	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF212	GRCh38.p7	4:1072458	TAACACATGGACTGC[G/T]CTGGTGGAGGATGAG	285498
rs189915724	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1061521	GCAGGGGGATCCAGC[A/G]CGGCCACAGAAGTGA	285498
rs189950882	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1097465	AAAAAATTAGCCGGG[C/T]GTGGTGACGGGCACC	285498
rs190132270	snp	A/G			intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1111843	ACAACCCAAAGGGCC[A/G]TGGACAGTGGAAACG	285498
rs190145033	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF212	GRCh38.p7	4:1093438	ACAATACCACCTCAC[A/G]TCACACAGCTGCGGG	285498
rs190152894	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1077122	AGTCCCAGCTACTCG[A/G]GAGGCTGAGGCAGGA	285498
rs190201588	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, synonymous-codon, downstream-variant-500B, nc-transcript-variant	RNF212	GRCh38.p7	4:1056494	TTTGAAATGACTTCA[A/G]AACTTCACACTGTTG	285498
rs190203919	snp	C/T	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	TMED11P, LOC105374344, RNF212	GRCh38.p7	4:1115756	TAGGCCAAGCACTTG[C/T]ATGCCTTATTTGCTT	285498
rs190211771	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1082750	GGCTTACTCCGAATT[A/G]CCAGCCCCCAGAACA	285498
rs190212433	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1079340	AACATGGGACCTGTA[C/T]GGGAACAACACAGGA	285498
rs190281764	snp	A/T	0.00279162	0.0372561	intron-variant	RNF212	GRCh38.p7	4:1092453	ACACCAGCCTCCAGG[A/T]CTCCATTAGGGGGAG	285498
rs190441787	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1076337	CAGCTGTGCCCCAGG[C/T]GCTGTCATGGGATGG	285498
rs190450354	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1102657	GGAGATCGAGACCAT[C/T]CTGGCTAACATGGTG	285498
rs190589493	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1087983	TCAGGTAGTTCTTTA[C/T]AGGAGTGTGATAATG	285498
rs190735018	snp	A/G	0.000183479	0.00957631	intron-variant	RNF212	GRCh38.p7	4:1085863	GGCAGTGGGTGCCTC[A/G]ACTGCGCACTCACGG	285498
rs190746043	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1067094	CCATTGAATAGTGTG[C/T]TTTGTTTTGAGGACA	285498
rs190833204	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1104472	GCAGTGGAGGGCTGT[C/T]CAGGAGGCTGTTTTT	285498
rs190891424	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1080445	CAGAGTGGTCCATCC[A/G]GACACTTGCCTCCCA	285498
rs190904341	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1104039	GGTCACTAGAGACAG[C/T]TAAGAAAATCCATTG	285498
rs190915902	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1084706	CACTCCAGCCTGGGT[A/G]ACAGAGGAAGACCCT	285498
rs190927618	snp	C/T	0.0217236	0.101931	intron-variant	RNF212	GRCh38.p7	4:1066018	AGCTAGGACTACAGG[C/T]GCGATTTTTTAAATA	285498
rs191055716	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1088475	TAAAATTGGAACTTA[C/T]GTTTAAAAGGGAAGC	285498
rs191072507	snp	A/C	0.00279162	0.0372561	intron-variant	RNF212	GRCh38.p7	4:1080902	ACATGAGGTTGGGCT[A/C]CCTGTGCCAGAGTGA	285498
rs191074765	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1107789	TTTTCTGTACTATAC[A/G]AATGTTGTGTAACTT	285498
rs191079027	snp	A/G	0.00199481	0.0315187	intron-variant	RNF212	GRCh38.p7	4:1062005	TCCAGAGCGGCTACC[A/G]TAAATGAGCCAAAGA	285498
rs191131820	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1098855	GGGAACTGTCACTGT[C/T]ATCTAAGGTATATTA	285498
rs191150116	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1061681	GTAAAGACAGGCGGA[C/T]ACCCCGGGACATCTC	285498
rs191205405	snp	C/G	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1105085	GCCTCAGCTTTCAGG[C/G]CCTTCACCCTCAAGA	285498
rs191254291	snp	A/C	0.242775	0.249896	intron-variant	RNF212	GRCh38.p7	4:1096572	ACAGAACCAAGCACA[A/C]CTCCCACAGCTCCAT	285498
rs191281847	snp	A/G	0.00199481	0.0315187	intron-variant	RNF212	GRCh38.p7	4:1108552	GATGAGGCTGTGGGT[A/G]CTGGTACAGTTGGAA	285498
rs191306553	snp	C/G			utr-variant-3-prime, intron-variant	RNF212	GRCh38.p7	4:1071504	GATACATATTTATCT[C/G]ATAAGGAAATGTCAT	285498
rs191537290	snp	A/C/T	0.00199529	0.0315338	downstream-variant-500B, intron-variant	RNF212	GRCh38.p7	4:1071044	AAAAACTAATTTTTT[A/C/T]AAATACTGTTATTAC	285498
rs191662707	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1062594	CAGGAACAGAACAAA[C/G]ACAAGGATGTCTGTT	285498
rs191698640	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1111315	TAGGATTATTATCCC[A/G]TATTAATCGCTCCCC	285498
rs191715651	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1076547	GCCAGAGAGTGAGAC[C/T]TCAGTCTGCACAGGC	285498
rs191735451	snp	C/T	0.00398564	0.0444627	intron-variant	RNF212	GRCh38.p7	4:1101319	TTTATTATTGGTAGA[C/T]AATACTGAGCAGAAT	285498
rs191788993	snp	A/T	0.00279162	0.0372561	intron-variant	RNF212	GRCh38.p7	4:1078728	CGGGACCAACATGGG[A/T]CCAGCAGAGGATCAA	285498
rs191797292	snp	C/T	0.00159617	0.0282053	intron-variant	RNF212	GRCh38.p7	4:1060072	CCATTGCACTCCAGC[C/T]TGGGCAACAAGAGCG	285498
rs191845789	snp	C/G	0.00199481	0.0315187	intron-variant	RNF212	GRCh38.p7	4:1095184	CATGGTCTCGGGATA[C/G]CGCACCTGGCTCATC	285498
rs191856184	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF212, LOC105374344	GRCh38.p7	4:1114435	CGGTAGCTACGGGCC[A/G]AGTGACCCCTGCGCC	285498
rs191857987	snp	A/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1058164	AAATTTTTAGCACTA[A/T]TTCTCTCTGGTGAGT	285498
rs191987816	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1099976	GATGCAGCCACTGCC[G/T]CTAGGCAGGAACGGG	285498
rs191997320	snp	A/G	0.00557542	0.0525036	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1092827	AGAGTCAAGGCAGTC[A/G]GGGGAGAATGCAGGT	285498
rs192018387	snp	C/T	0.00755907	0.0610114	intron-variant	RNF212	GRCh38.p7	4:1057309	GCATCAAAAGCCACT[C/T]AAGGGCTCTGGGGGG	285498
rs192152592	snp	A/T	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1077257	AAACAAAAAACAAAA[A/T]GCAAAAGACAGAAAA	285498
rs192249422	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1106972	AAAAAATCCAAAGGC[C/T]CACTGATAGGAAAAT	285498
rs192334979	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1077947	GCAGGGAGAGGATGC[A/G]TGTGCTTGACCCAAC	285498
rs192343182	snp	A/T	0.00199481	0.0315187	intron-variant	RNF212	GRCh38.p7	4:1058652	TTTAATCTTTCTACC[A/T]TTATGCACCTCTGCA	285498
rs192347704	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1068389	TGCTTTACAACGTCA[C/T]GTAAAAATCCCTCTT	285498
rs192427438	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1106335	GCCTTTTTAAACACC[A/G]ATCAAATATGAACAA	285498
rs192495486	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1063571	CCAGGTGTGGTGGTG[C/T]GCACCTGTAATCCCA	285498
rs192502484	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1082254	TGGACTGATCTCCAC[C/G]ATGGCCAGTAGCAGA	285498
rs192587106	snp	A/G	0.0107246	0.0724382	intron-variant	RNF212	GRCh38.p7	4:1102777	GAATGGCGTGAACCC[A/G]GGAGGTGGAGCTTGC	285498
rs192600843	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1082986	TGGGTGGCACGAACG[A/C]CACCACAGTGAGGCC	285498
rs192647218	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1089796	GGCAGTTCCCCCTGC[A/C]CTCTCTCCTGCTGTT	285498
rs192728018	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1067847	CACTCCAGCCTGGGC[A/G]ACACAGCGAGACTCT	285498
rs192796116	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1101794	AAATATCTGTACATA[C/T]ACCTAAGAAAGCTTG	285498
rs192806312	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1063120	GTGTTAGTATTAGAT[A/G]GCAATACCCCCTACA	285498
rs192874095	snp	C/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1110172	CGGCCAAAAGACAAA[C/G]GGATTGATGCCTGAT	285498
rs192882242	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1074662	CTGCTTGGCATGGCC[C/G]TCTGAGCTGCCTGCA	285498
rs192924988	snp	A/G/T	0.291704	0.247026	intron-variant	RNF212	GRCh38.p7	4:1086651	GAGGAGGGGGTGGGG[A/G/T]GACAGAAGAGGGGTG	285498
rs192985269	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1087251	GTAGGGGAGAGAGGA[C/T]GGGGTAGGGGAGAGA	285498
rs192989269	snp	A/G/T	7.45078e-05	0.00610321	utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant	RNF212, LOC105374344	GRCh38.p7	4:1113476	CCATGCCAGGCGGGC[A/G/T]ACCGCAGCGGCGAGG	285498
rs193063713	snp	A/G	0.000263535	0.011476	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RNF212	GRCh38.p7	4:1096834	TGCCTGGATATCTGC[A/G]TCGGTCTGAAAGAGA	285498
rs193102813	snp	A/G	0.000149005	0.00863021	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1073570	ATCGATGCATGTATC[A/G]GTCTGAGGTTACAGG	285498
rs193197832	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1068959	ACACCTGCAATCCTA[C/G]CACTTTGGGAGGCTG	285498
rs193231186	snp	A/G			upstream-variant-2KB, intron-variant	RNF212, TMED11P, LOC105374344	GRCh38.p7	4:1115056	AGACTCAGTCTCAAA[A/G]ATAAGTTTAAGAATA	285498
rs193255340	snp	C/G	0.00279162	0.0372561	intron-variant	RNF212	GRCh38.p7	4:1089280	GGATGTGAGACATTG[C/G]GTAAAAGGATAAATT	285498
rs199600360	snp	A/G	0.000100078	0.00707313	missense, utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1072941	GCGGGTGTTCTGAAC[A/G]TGTCCAGGGTGCCCT	285498
rs199652198	snp	C/T	1.65146e-05	0.0028735	intron-variant	RNF212	GRCh38.p7	4:1081373	AGGCAGGTGCAGAAT[C/T]GGAAAGACCTGCAGG	285498
rs199681793	in-del	-/AGACCAACATG			intron-variant	RNF212	GRCh38.p7	4:1079287	CACAGGGTCAACACA[-/AGACCAACATG]GGACCAACATAGATT	285498
rs199734209	snp	C/T	0.00199792	0.0315431	synonymous-codon, missense, intron-variant, nc-transcript-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1073066	GAACGCTAGGAGGAG[C/T]AGCCAGTGAGGACAG	285498
rs199811548	snp	A/G	1.65982e-05	0.00288077	missense, intron-variant, nc-transcript-variant	RNF212	GRCh38.p7	4:1081584	GAAACTGAACTTTTT[A/G]TTGTGCTGAAAGCTG	285498
rs199814803	snp	G/T			utr-variant-3-prime, intron-variant	RNF212	GRCh38.p7	4:1072234	AAAGATCAGTGGCTG[G/T]CAAGGGTTGGTGGGA	285498
rs199880036	snp	A/G	8.23703e-05	0.00641704	synonymous-codon, missense, intron-variant, nc-transcript-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1073036	GTTGGTGAGTTCCCC[A/G]TGCCTTCCAGAACTG	285498
rs199926869	in-del	-/TT	0.00874735	0.0655527	intron-variant	RNF212	GRCh38.p7	4:1082006	CCATCATCCCAACAC[-/TT]TGGGAGGCAGGGGCG	285498
rs199970026	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1080943	GGCATAGCCTGGAGA[A/C]GGGGCAGACACAAGC	285498
rs199971163	in-del	-/TTT			intron-variant	RNF212	GRCh38.p7	4:1070906	ATACTGTTCTTACAA[-/TTT]TTTCTGTGTGCTTGA	285498
rs199980229	snp	G/T	0.00398564	0.0444627	upstream-variant-2KB, intron-variant	RNF212, TMED11P, LOC105374344	GRCh38.p7	4:1115430	CGGAAAAGAAGTAGG[G/T]TTAGTGTCATAAAGT	285498
rs200022451	in-del	-/CC			intron-variant	RNF212	GRCh38.p7	4:1095514	AACCAAGCACAACTC[-/CC]ACAGCTCCATGGTCT	285498
rs200058471	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1107578	CCTCAGCCTCCCAAG[C/T]AGCTGGGACTACAGG	285498
rs200133253	snp	A/C	0.000379478	0.0137694	missense, intron-variant, downstream-variant-500B, nc-transcript-variant	RNF212	GRCh38.p7	4:1073170	ACCATGGGATGAAAC[A/C]GAAAGAAGCTGTTAG	285498
rs200208503	snp	G/T			intron-variant	RNF212	GRCh38.p7	4:1068789	TGAATGTATTTAGTC[G/T]TCATTTTAAAATGTT	285498
rs200326254	in-del	-/T			intron-variant	RNF212	GRCh38.p7	4:1070879	GATGTTGGAGTTTTG[-/T]TTTTTTTTTTAATAC	285498
rs200415933	snp	C/T	0.000399281	0.0141238	missense, synonymous-codon, intron-variant, nc-transcript-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1073022	GGAAGTGTTTTAGAG[C/T]TGGTGAGTTCCCCGT	285498
rs200445136	in-del	-/TTCC	0.00199481	0.0315187	intron-variant	RNF212	GRCh38.p7	4:1100197	ACCAGGCTTACTGCT[-/TTCC]CGTGATACTTCTAGC	285498
rs200537629	in-del	-/G			intron-variant	RNF212	GRCh38.p7	4:1092515	TGGTTTGTCTGGCCT[-/G]GGCTCTGACCAATGT	285498
rs200556599	in-del	-/GGGACCAACAC			intron-variant	RNF212	GRCh38.p7	4:1079264	ACACAGGACCAACAT[-/GGGACCAACAC]AGGGTCAACACAAGA	285498
rs200627313	snp	A/C	8.27835e-05	0.00643311	missense, intron-variant, nc-transcript-variant	RNF212	GRCh38.p7	4:1079671	GAAGGAGAGAGATCA[A/C]CTTCCATCGACTCCA	285498
rs200631846	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1079287	CACAGGGTCAACACA[A/G]GACCAACATGGGACC	285498
rs200676613	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1110854	TCCCGACATGCAGCA[C/T]CTGTGGCTTTTTGGA	285498
rs200680799	snp	C/T	0.000216614	0.0104048	intron-variant	RNF212	GRCh38.p7	4:1085888	TCACGGGGGGTGGGG[C/T]GCCTTACCTTTGTAG	285498
rs200772374	in-del	-/AAGCACAAC			intron-variant	RNF212	GRCh38.p7	4:1095385	GCTCATCACAGAACC[-/AAGCACAAC]TCCCACAGCTCCATG	285498
rs200805960	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1090763	AAAATTCAAGTGGCA[A/T]TGAATCAATTCCACT	285498
rs200835789	snp	C/T	0.00557542	0.0525036	intron-variant	RNF212	GRCh38.p7	4:1059018	ATGAAAGGGGAGATG[C/T]GACGACTGAGTTCTC	285498
rs200888142	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1109836	TCACTTGTGTATCCA[C/T]ACTCGCCTCAGTGTC	285498
rs200988570	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1067231	CTCAAATCAGTCTAT[A/G]GCAAAATGGTATGAT	285498
rs201010981	in-del	-/C			intron-variant	RNF212	GRCh38.p7	4:1096745	CATCACGGAACCAAG[-/C]CACACCCCTCACAGC	285498
rs201016366	snp	C/T	0.00598191	0.0543615	intron-variant, synonymous-codon, downstream-variant-500B	RNF212	GRCh38.p7	4:1093547	AGCCTGTGACCTCCA[C/T]GGCCCATGCCGGAAG	285498
rs201027038	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1075660	TAAACTATATCAGCT[A/G]GTTTCCCTCATTAAC	285498
rs201072260	in-del	-/CG			intron-variant	RNF212	GRCh38.p7	4:1067603	GTGCAATGGCTCACA[-/CG]CCTGTAATCCCAGCA	285498
rs201086172	snp	C/G	6.67167e-05	0.00577528	intron-variant	RNF212	GRCh38.p7	4:1085867	GTGGGTGCCTCGACT[C/G]CGCACTCACGGGGGG	285498
rs201164859	in-del	-/A			intron-variant	RNF212	GRCh38.p7	4:1073950	TAGGAATTTTAGGTG[-/A]AAAAAAAACAAAATT	285498
rs201173213	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1090060	AGGACAGGGTGGTGG[C/T]AGCAAGATGGCCTGA	285498
rs201178648	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1076781	AGGGGTTGGCAAACT[A/G]TGGCCTGCAGCCTGT	285498
rs201230381	snp	A/C/G	0.00232941	0.0340482	missense, upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant	RNF212, LOC105374344	GRCh38.p7	4:1113412	GTGAGGCTGAAGCAC[A/C/G]ACGTCCTGTGGGGCG	285498
rs201319741	in-del	-/A			utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1072617	TGATTTAAGTATGTG[-/A]AAAAAAAAACTCCCT	285498
rs201347530	snp	A/C	0.00358779	0.0422022	intron-variant	RNF212	GRCh38.p7	4:1079251	CAACACAGGGTCAAC[A/C]CAGGACCAACATGGG	285498
rs201468501	snp	A/G			utr-variant-3-prime, intron-variant	RNF212	GRCh38.p7	4:1072284	GGTGGCGCACAGAGG[A/G]TTTTTAGGGTGTGGC	285498
rs201470853	in-del	-/CAACACAGGAC			intron-variant	RNF212	GRCh38.p7	4:1078939	GGACCAACACAGGGT[-/CAACACAGGAC]CAACACAGGACCAAC	285498
rs201543039	snp	A/G	1.6476e-05	0.00287014	missense, utr-variant-3-prime, intron-variant, nc-transcript-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1073008	CCTCAGCATATATTG[A/G]AAGTGTTTTAGAGTT	285498
rs201591785	snp	C/G	0.00199481	0.0315187	intron-variant	RNF212	GRCh38.p7	4:1100201	GGCTTACTGCTTTCC[C/G]GTGATACTTCTAGCG	285498
rs201635971	in-del	-/AAACAAAC			intron-variant	RNF212	GRCh38.p7	4:1083640	GAGACTCTGTCTCAA[-/AAACAAAC]AAACAAACAAACAAA	285498
rs201684537	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1108438	CTTTATTATATTAGA[C/T]TGACTACTACTTTTA	285498
rs201721758	in-del	-/AA			intron-variant	RNF212	GRCh38.p7	4:1102989	CTACTAAAAAAATAC[-/AA]AAAAAAAAAAAATCA	285498
rs201861210	snp	C/T	0.000164799	0.00907592	intron-variant	RNF212	GRCh38.p7	4:1096873	ACTCTACATTTATTG[C/T]GTCTAATAAACGCTT	285498
rs201861273	snp	A/G	0.00697557	0.0586441	upstream-variant-2KB, intron-variant	RNF212, TMED11P, LOC105374344	GRCh38.p7	4:1115429	GCGGAAAAGAAGTAG[A/G]TTTAGTGTCATAAAG	285498
rs201932997	in-del	-/CCCCTCATA			intron-variant	RNF212	GRCh38.p7	4:1096690	ACAGAACCAAGCACA[-/CCCCTCATA]GCTCCATGGTCTCGG	285498
rs201936790	in-del	-/ACAC			intron-variant	RNF212	GRCh38.p7	4:1106250	TAAACAATTTTACTT[-/ACAC]ACACACACACACACA	285498
rs201978961	snp	A/T			intron-variant	RNF212	GRCh38.p7	4:1065325	AAAAATGATTACAAT[A/T]AACATTTATTTAAAG	285498
rs202129395	snp	C/T	8.27931e-05	0.00643348	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1073569	AATCGATGCATGTAT[C/T]GGTCTGAGGTTACAG	285498
rs202178770	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1099645	AATGTTTTCTTTTCG[C/T]ATTTAATTTTTAAAA	285498
rs202190932	in-del	-/AGGACCGACAT			intron-variant	RNF212	GRCh38.p7	4:1078791	ATACAGGGTCAACAC[-/AGGACCGACAT]GGGACCAACACAGGG	285498
rs367577034	snp	A/G	1.65097e-05	0.00287308	intron-variant	RNF212	GRCh38.p7	4:1081496	GACGAAAATGCCAGC[A/G]TCAGTGCACACAGTG	285498
rs367624418	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1102595	AAAACACAAAAAAAC[A/C]AAAAAAAAACACTTT	285498
rs367631908	snp	C/T	0.00676609	0.0577691	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1058001	AGGAGGCGGAGGTTG[C/T]GGTGAGCCAAGATGG	285498
rs367651991	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1081258	TGGGACCTGAGCCTC[C/G]CAGGGAGATGAAATA	285498
rs367719640	multinucleotide-polymorphism	AA/CG			intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1092975	GTCCACATGAGCTCC[AA/CG]ACTACGCCAGGACCA	285498
rs367774235	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1078399	TGCCTGGTGTGTGGC[C/T]GATGTGGTACATCTG	285498
rs367776205	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1064652	TTGAAAATTTATGAT[A/G]ATACAGTTTCCTACC	285498
rs367781069	snp	C/T	1.64961e-05	0.00287189	intron-variant	RNF212	GRCh38.p7	4:1096890	TCTAATAAACGCTTC[C/T]GGCCCCCAGTTAAAA	285498
rs367797344	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1077070	AGGTCTCTACTAAAA[A/G]TACAAAAATTAGCCA	285498
rs367803304	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1097314	AGGTTTAAGAAACAG[C/T]GTCTCGTAGGTCGGG	285498
rs367810629	snp	C/T	0.00018141	0.00952218	utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant	RNF212, LOC105374344	GRCh38.p7	4:1113493	CCGCAGCGGCGAGGC[C/T]GGGCCCACGCGAAGC	285498
rs367832540	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1107305	ATCCGCCTGCCTCAG[C/T]CTCCCAAAGTGCTGG	285498
rs367842216	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1085510	TTCGCAAACGGCTAC[A/G]ACTCCTGGCAGAAAG	285498
rs367884709	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1095820	CCCCCCACAGCTCCA[C/T]GGTCTCGGGATAGCG	285498
rs367988661	snp	A/G	1.64773e-05	0.00287026	missense, utr-variant-3-prime, intron-variant, nc-transcript-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1073004	TGTACCTCAGCATAT[A/G]TTGGAAGTGTTTTAG	285498
rs367993931	snp	A/G	0.000181427	0.00952263	synonymous-codon, intron-variant, nc-transcript-variant	RNF212	GRCh38.p7	4:1081424	ACCCACACACCTGTC[A/G]GGGGCTGATGAGTGA	285498
rs368058443	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1085777	TTTCTGGTAAATGAA[C/T]GAGCTCTTCCCTCTG	285498
rs368072313	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1060304	ATCAGCCCGCTGTGT[C/G]TCCCACAGGGCTTGG	285498
rs368128599	snp	G/T			intron-variant, missense, downstream-variant-500B	RNF212	GRCh38.p7	4:1093807	GGGTGAGGGGGTGAG[G/T]TGCGTCCTGGATGGT	285498
rs368197042	snp	C/T	1.64977e-05	0.00287203	intron-variant	RNF212	GRCh38.p7	4:1096730	ATAGTGCACCTGGCT[C/T]ATCACGGAACCAAGC	285498
rs368243601	snp	C/T	3.30852e-05	0.00406712	intron-variant	RNF212	GRCh38.p7	4:1079594	GAGGAAAATGGGAAA[C/T]GCCACACGTCTGGTA	285498
rs368264047	snp	A/G	0.00993419	0.0697739	intron-variant	RNF212	GRCh38.p7	4:1108121	CCAGGAACACAGCAC[A/G]ATTCAACAACCTAGG	285498
rs368267495	snp	C/T	0.00438332	0.0466095	intron-variant	RNF212	GRCh38.p7	4:1099170	CACATTGCAGAGGGC[C/T]GGCGATAAGCCAGGT	285498
rs368279132	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1069260	ATAAATTAGTGAATA[C/T]ATAGATACCTGAATT	285498
rs368346002	snp	A/G	0.000292227	0.0120842	intron-variant, missense, downstream-variant-500B	RNF212	GRCh38.p7	4:1093938	TGGCTTCCATGGGTC[A/G]AGCCTCTGGGCACCT	285498
rs368409955	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1104347	TTCTTGCCCATACAA[C/T]AGTTCAAGACCAGGC	285498
rs368412905	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1064489	AGAAGTTTATTTCTC[A/G]CAGTTCTGGAGACTG	285498
rs368568947	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1066569	CTCCTGAGCTCAAGC[A/G]ATCCTTTTGCCTTGG	285498
rs368575545	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1080957	ATGGGGCAGACACAA[A/G]CCACAGGACATGTGC	285498
rs368602483	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1074004	AAATTCTGAGTAAAT[A/C]ATTCTTGGGTGCATA	285498
rs368612896	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1095239	GCTCCATGGTCTCGG[C/G]ATAGCGCACCTGGCT	285498
rs368627425	snp	C/T	1.6483e-05	0.00287076	intron-variant	RNF212	GRCh38.p7	4:1096753	AACCAAGCCACACCC[C/T]TCACAGCTCACCTGG	285498
rs368648811	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1101642	ATCATCTGCTACATC[A/G]TCATCTATTGCTCCT	285498
rs368650125	snp	A/G	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1070695	CTGTGCTGTGTCAAC[A/G]TGGGTGCCTGGCCAG	285498
rs368655575	snp	C/T			downstream-variant-500B	RNF212	GRCh38.p7	4:1055941	CACGCAGGCCGCATC[C/T]GCAGGGTGAGCTCAG	285498
rs368689824	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1074647	GAAGGACGGACCCCC[C/T]TGCTTGGCATGGCCC	285498
rs368694444	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1075717	GTTTCACTGTCGTCC[A/C]GGCTGGAGTGCAGTG	285498
rs368837566	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1096653	CAGCTCCATGGTCTC[A/G]GGATAGTGCACCTGG	285498
rs369008108	snp	A/G	8.27684e-05	0.00643252	missense, intron-variant, stop-gained, nc-transcript-variant	RNF212	GRCh38.p7	4:1079653	CTTACTTTTCTAATC[A/G]GAGAAGGAGAGAGAT	285498
rs369029832	snp	C/G	0.0240643	0.107019	upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime	RNF212, LOC105374344	GRCh38.p7	4:1113660	GCACCTGGGAGGGCG[C/G]GTGTGACTCGTCTCC	285498
rs369042634	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1070833	GGAGCAAATTAACAA[A/C]ATGTTAACATTTGGG	285498
rs369048108	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1095303	ATGGTCTCGGGATAG[C/T]GCACCTGGCTCATCA	285498
rs369198728	snp	C/G			utr-variant-3-prime, intron-variant	RNF212	GRCh38.p7	4:1071885	AAAACTAAACACCCT[C/G]TCACCATCTGATCCA	285498
rs369225551	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1111002	TGACCTCAAAAGCTA[C/T]GACGCTCTGAGCCCT	285498
rs369239691	in-del	-/CAGT			intron-variant	RNF212	GRCh38.p7	4:1106289	ACACACACACACACA[-/CAGT]CACTCAGACACAGAG	285498
rs369241654	snp	C/G/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1078454	AGACGACGGGAGAGC[C/G/T]GGGCCTGGACTCTCC	285498
rs369246369	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1057486	ACTGTGGTCTGTTCC[C/G]GGGCTGGGGCTGAGT	285498
rs369272787	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF212, LOC105374344	GRCh38.p7	4:1114538	TTACATGTTAACATG[A/G]TATTTTTGATATATT	285498
rs369299534	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1067586	TGAAATACCTAGGGC[C/T]GGGTGCAATGGCTCA	285498
rs369328789	snp	A/C/T			intron-variant	RNF212	GRCh38.p7	4:1078889	AACACAGGACCGACA[A/C/T]GGGACCAACACAGGG	285498
rs369339393	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1057127	ATCTCTGAGAACCTC[A/G]GAGCAGCACGCACAC	285498
rs369341283	in-del	-/TCT	0.00159617	0.0282053	upstream-variant-2KB, nc-transcript-variant, intron-variant	RNF212, TMED11P, LOC105374344	GRCh38.p7	4:1115268	TAATATTTTAAACAA[-/TCT]TCTTAGCTATAAAGA	285498
rs369382296	snp	C/G/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1099549	GAGAGCTGAGGCCCT[C/G/T]GCATCATCAAGAAAA	285498
rs369406370	in-del	-/TAGAAACAGGCACTTCCTTT			intron-variant	RNF212	GRCh38.p7	4:1110370	TGTCACTACAGGGAA[-/TAGAAACAGGCACTTCCTTT]GTGCCTGTTTGGGTC	285498
rs369413262	snp	A/G	3.31219e-05	0.00406938	intron-variant	RNF212	GRCh38.p7	4:1079700	CAGTCTGTTAAACAC[A/G]TAGTGAAAGGCTTTG	285498
rs369413999	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1087740	TGGGGGAGGTGATTG[A/G]ATCATGGGGGTGCTT	285498
rs369455177	snp	G/T			intron-variant	RNF212	GRCh38.p7	4:1092348	GACCTGAGCAGCAGA[G/T]GGGGTGAGTTCTACT	285498
rs369457393	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1062800	GACATGATTTGCCAT[A/G]TACAGAAAACCCTAG	285498
rs369580247	snp	C/G	3.33689e-05	0.00408453	intron-variant	RNF212	GRCh38.p7	4:1085852	CCAATGCACATGGCA[C/G]TGGGTGCCTCGACTG	285498
rs369646291	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1079744	CTTACCTCTAACAAC[A/G]TCAGTTGAAATACAC	285498
rs369664150	snp	C/T	0	0	intron-variant	RNF212	GRCh38.p7	4:1096174	CCCCCCACAGCTCCA[C/T]GGTCTCGGGATAGCG	285498
rs369692308	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1075452	AGGCGCGTTGCAGGG[C/T]GAGCAGGCAAGAGAC	285498
rs369795061	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1092607	AACAAAGTTTAAAAG[A/G]GACAGTGAGTGTTTA	285498
rs369816429	snp	A/C	0.00438332	0.0466095	intron-variant	RNF212	GRCh38.p7	4:1079063	TCAACACAGGACCAA[A/C]ATGGGACCAACACAG	285498
rs369852572	snp	C/G			upstream-variant-2KB, intron-variant	RNF212, TMED11P, LOC105374344	GRCh38.p7	4:1114971	TACTCGGGAGGCTGA[C/G]GTGGGAGGATTGCTT	285498
rs369975404	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1110807	TCCACCCCTTTTCAC[C/G]ACTTTTTTGTGTGTC	285498
rs369995204	in-del	-/AGCTCCCGACTACGCCAGGAC			intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1093039	GTAGGGCAGAGGCTG[-/AGCTCCCGACTACGCCAGGAC]GGTGGATGGAACGGA	285498
rs370009317	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1078212	ATAAGCCAATAACTG[A/G]CACTGTGGAACACAG	285498
rs370025560	in-del	-/GAG			intron-variant	RNF212	GRCh38.p7	4:1074780	ATCTTGTGAAATCAG[-/GAG]CTTTTGTCTCTGTAC	285498
rs370043717	snp	C/T	4.9666e-05	0.00498302	missense, utr-variant-5-prime, intron-variant, nc-transcript-variant	RNF212	GRCh38.p7	4:1108365	GAAAGCAAAACTGTA[C/T]GACAAGGAGCTTTAC	285498
rs370048860	snp	C/T	0.00199481	0.0315187	intron-variant	RNF212	GRCh38.p7	4:1097379	GGAGGCCGAGGCGGG[C/T]GGATCACAAGGTCAG	285498
rs370051508	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1073399	ATCTCCTGTGACTTG[C/T]TACACGGTCATCAGG	285498
rs370064877	snp	G/T			intron-variant	RNF212	GRCh38.p7	4:1083100	ATGCAGGCGATACCA[G/T]GTATGTAGAGAGTGG	285498
rs370107437	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1107205	TACAGGCGTGTGCCA[C/T]CATGCCCAGCTAATT	285498
rs370207238	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1106774	GGCAGGCACTGAGCC[C/T]CTAAGCTGCCACATG	285498
rs370216464	snp	A/C/T	4.80931e-05	0.00490349	intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1113342	TCTCCAGCCTGCGTT[A/C/T]GGGAAGCCCTGACCT	285498
rs370262003	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1095510	ACAGAACCAAGCACA[A/C]CTCCCACAGCTCCAT	285498
rs370278943	snp	A/G	0.00438332	0.0466095	intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1112067	AAAAAAATCAGGGGT[A/G]CGTGGCTGCACATGC	285498
rs370386443	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1096535	CAGCTCCACGGTCTC[A/G]GGATAGTGCACCTGG	285498
rs370399772	snp	C/T	4.11717e-05	0.00453698	intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1113314	CCCTGACCCCCTTGC[C/T]GCTCCCCTCCCCTCT	285498
rs370468226	snp	C/T	0.0023933	0.0345097	downstream-variant-500B, intron-variant	RNF212	GRCh38.p7	4:1071427	TAGAAGAATTCTGTT[C/T]TGTGAAAGATAATGT	285498
rs370549678	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF212, TMED11P, LOC105374344	GRCh38.p7	4:1115169	CAATCTCTGGTATCT[C/T]TGAAATCATAAAAAT	285498
rs370590742	snp	A/G	1.72946e-05	0.00294058	synonymous-codon, upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant	RNF212, LOC105374344	GRCh38.p7	4:1113438	GGGCGGCTGGAAGCA[A/G]CGATTACAGAACACC	285498
rs370595034	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1059721	AAACAAAACCCTGTA[A/C]ATTGAACACACAGAA	285498
rs370624541	snp	C/T	1.64974e-05	0.00287201	synonymous-codon, intron-variant, nc-transcript-variant	RNF212	GRCh38.p7	4:1090803	TCTATAGAAGGCTAA[C/T]AATCTCTTCCTGTGT	285498
rs370652671	snp	C/T	0.00438332	0.0466095	intron-variant	RNF212	GRCh38.p7	4:1106947	GGTTGTTTGAAACAG[C/T]GAAAAACCGAAAAAA	285498
rs370664252	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1103086	TCATTATGGAACTTA[C/G]AGACATGAAAAATAT	285498
rs370672337	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1085687	AGGGGAAACCATTCA[C/T]CTCTTTTTCACTTTT	285498
rs370777761	snp	C/T	6.59859e-05	0.00574357	intron-variant	RNF212	GRCh38.p7	4:1096735	GCACCTGGCTCATCA[C/T]GGAACCAAGCCACAC	285498
rs370802233	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1102989	CTACTAAAAAAATAC[A/C]AAAAAAAAAAAAATC	285498
rs370853206	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1076285	AGCAGCAAGGGTGGA[A/G]GAGGAAGGAAAAGAA	285498
rs370855797	snp	G/T	0.021333	0.101051	intron-variant	RNF212	GRCh38.p7	4:1111534	GTGAAACCCTGTCCA[G/T]TTCTCTAGCCCTTGT	285498
rs370871425	snp	A/G	0.0146672	0.084371	intron-variant	RNF212	GRCh38.p7	4:1109199	TTTTAGTAGAGACAG[A/G]GTTTTGCCATGTTGG	285498
rs370894763	snp	C/T	0.00438332	0.0466095	intron-variant	RNF212	GRCh38.p7	4:1059394	TTCTGTCTTGTATCA[C/T]GGTTTGGCATCTGGA	285498
rs370993216	snp	A/G	0.00438332	0.0466095	intron-variant	RNF212	GRCh38.p7	4:1077303	TTTGCCCCTCACTTA[A/G]GAACTTTGATTCATT	285498
rs371006588	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1096601	ATGGTCTCGGGATAG[C/T]GCACCTGGCTCATCA	285498
rs371043312	snp	C/G/T	0.000798403	0.0199641	utr-variant-3-prime, intron-variant	RNF212	GRCh38.p7	4:1072214	GTCTGAAAAAGGGAC[C/G/T]GTAAAAAGATCAGTG	285498
rs371093790	snp	A/T			intron-variant	RNF212	GRCh38.p7	4:1081088	AGGTCAGCCCCTTAA[A/T]TTCCTGTTAGGGCAG	285498
rs371212537	snp	C/G/T	0.000214271	0.0103488	missense, intron-variant, downstream-variant-500B, nc-transcript-variant	RNF212	GRCh38.p7	4:1073152	GGGGCTTAGACAAGG[C/G/T]CAACCATGGGATGAA	285498
rs371215667	snp	A/G	0.00358779	0.0422022	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1058118	AACCTGACTCAAAGC[A/G]TGTAAAAACAGGGAT	285498
rs371245228	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1060756	TTCTGGAGGGGACCG[C/T]GTACTGAAGAGTGAG	285498
rs371288733	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1059164	CGTCGGGGGGTTGCC[A/G]GCTTGTGGGGCAGGA	285498
rs371316558	in-del	-/A			intron-variant	RNF212	GRCh38.p7	4:1062832	AATCCACAAAAAAAA[-/A]TCCCCAGAGCTCATA	285498
rs371330245	snp	C/T			intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1112688	GCCCGACCCCTGTGT[C/T]CCCCTCATCTTGCAT	285498
rs371347045	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1073779	CTCCCTCATCTTTAT[C/T]GCCCTCTGACAAGTT	285498
rs371414918	snp	A/C	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1111744	CTCCCAGGTTACACA[A/C]CCAACAGAAATGTGT	285498
rs371423387	snp	A/G	4.99929e-05	0.0049994	intron-variant	RNF212	GRCh38.p7	4:1085889	CACGGGGGGTGGGGC[A/G]CCTTACCTTTGTAGT	285498
rs371439615	snp	C/T	1.68434e-05	0.00290197	intron-variant	RNF212	GRCh38.p7	4:1073701	TGGGTAAAATTCCAA[C/T]ATTGCGGCTTACGAG	285498
rs371440842	snp	C/G	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1062582	TCCTCCTAAGATCAG[C/G]AACAGAACAAAGACA	285498
rs371457607	snp	A/C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1088884	CATGTGTGCAGAGGA[A/C/T]AAGAGCTGAGATTTG	285498
rs371466365	snp	A/T			intron-variant	RNF212	GRCh38.p7	4:1089931	TTATAAATTACCGAA[A/T]CTCAGGTTATTCTTT	285498
rs371621127	snp	C/T	0.00199481	0.0315187	intron-variant	RNF212	GRCh38.p7	4:1094968	TTAAGAAAGTAAAAA[C/T]TCAACCCACAGAAAT	285498
rs371629343	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1077160	TTGAACCCGGGAGGC[A/G]GAGGTTGCAGTGAGC	285498
rs371708757	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1107254	GACGGGGTTTTACCA[C/T]GTTAGCCAGGATGGT	285498
rs371708881	in-del	-/A			intron-variant	RNF212	GRCh38.p7	4:1078096	GATTACCCATGCCAC[-/A]GGGCTGCTACACGAC	285498
rs371748322	snp	A/G			synonymous-codon, nc-transcript-variant	RNF212	GRCh38.p7	4:1058389	GCCCAGGGAGGAGAC[A/G]CTGCCTGTGGTGGAA	285498
rs371774806	snp	A/G/T	3.30551e-05	0.00406528	intron-variant	RNF212	GRCh38.p7	4:1081526	GTGACTCAGCAACAT[A/G/T]CATCTCTATTTTGTT	285498
rs371780652	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1095230	CCCCCCACAGCTCCA[C/T]GGTCTCGGGATAGCG	285498
rs371784705	snp	C/T	0.00438332	0.0466095	intron-variant	RNF212	GRCh38.p7	4:1086142	CGGCCTTGGGGGCCA[C/T]GCAGAGCGAAGTCAA	285498
rs371785141	snp	A/G	3.29864e-05	0.00406105	missense, intron-variant, nc-transcript-variant	RNF212	GRCh38.p7	4:1081434	CTGTCGGGGGCTGAT[A/G]AGTGAGGTGGCAGCA	285498
rs371907074	snp	A/G			intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1113254	TCCGCAGCCCCCCAC[A/G]TGCCCCCATGGCCCT	285498
rs371940717	snp	A/G	0.000153988	0.00877328	intron-variant	RNF212	GRCh38.p7	4:1108329	AGATGCAGATACGAC[A/G]CATTTCAACTTACAT	285498
rs371944887	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1110464	CCACCCCGAAGAATA[C/T]ATTCCAAGGAAAAAA	285498
rs371965986	snp	G/T			intron-variant	RNF212	GRCh38.p7	4:1082543	GCTAGGAATAGGCAG[G/T]TGCACAACAGCTCAA	285498
rs371994771	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1067210	AACATATGAATTTTG[A/G]GGGGACTCAAATCAG	285498
rs372117752	snp	C/T	4.96471e-05	0.00498208	intron-variant	RNF212	GRCh38.p7	4:1090743	ATTTAAATCTAAAGG[C/T]CAAAAAAATTCAAGT	285498
rs372123253	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1069350	TGTGGAAATGGAAAA[A/G]CTGCTATGAGGCAGT	285498
rs372138671	snp	C/T	0.0134861	0.0810011	intron-variant	RNF212	GRCh38.p7	4:1096086	GCACCTGGCTCATCA[C/T]GGAACCAAGCACACC	285498
rs372151880	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1104932	GGCATTTGAGGATGG[C/G]TGCTGGGGGCTCCTC	285498
rs372156034	snp	A/T	0.000153988	0.00877328	missense, intron-variant, nc-transcript-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1073023	GAAGTGTTTTAGAGT[A/T]GGTGAGTTCCCCGTG	285498
rs372173838	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1062394	TCTATGAACACATCA[C/T]GGTAACAGAACAAAA	285498
rs372218840	snp	A/G	0.000798403	0.0199641	intron-variant, synonymous-codon, downstream-variant-500B	RNF212	GRCh38.p7	4:1093553	TGACCTCCACGGCCC[A/G]TGCCGGAAGCCTGAG	285498
rs372230431	snp	A/G			utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant	RNF212, LOC105374344	GRCh38.p7	4:1113538	GACCAGCCTCCCCGC[A/G]CAGGGCCCGAAGGCG	285498
rs372299765	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1080836	TTGTGCCTTCCATCT[A/G]AAGAGCTAGGAGCTA	285498
rs372300743	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1101479	TTTTGTTCATCTGCT[C/T]CTGTTGAAGGATTAT	285498
rs372319522	snp	A/T			utr-variant-3-prime, intron-variant	RNF212	GRCh38.p7	4:1072285	GTGGCGCACAGAGGA[A/T]TTTTAGGGTGTGGCA	285498
rs372331560	snp	C/T	0.000413753	0.0143773	synonymous-codon, intron-variant, missense, nc-transcript-variant	RNF212	GRCh38.p7	4:1079652	ACTTACTTTTCTAAT[C/T]GGAGAAGGAGAGAGA	285498
rs372379232	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1101641	CATCATCTGCTACAT[C/G]GTCATCTATTGCTCC	285498
rs372390304	snp	C/T	1.64825e-05	0.00287071	intron-variant	RNF212	GRCh38.p7	4:1096757	AAGCCACACCCCTCA[C/T]AGCTCACCTGGGAGG	285498
rs372395699	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1092331	GGGAAAGTCTCCAAG[A/G]GGACCTGAGCAGCAG	285498
rs372405148	snp	C/T	0.000153988	0.00877328	intron-variant	RNF212	GRCh38.p7	4:1079622	GTATACAGAGGAACT[C/T]AGCAGGAGAGATGCA	285498
rs372416244	snp	A/G	0.00159617	0.0282053	intron-variant	RNF212	GRCh38.p7	4:1097562	GTGAGCCGAGATTAC[A/G]CCACTGCACTCCAGC	285498
rs372431632	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1108128	CACAGCACGATTCAA[C/T]AACCTAGGAATAAGG	285498
rs372453159	in-del	-/CTT			intron-variant	RNF212	GRCh38.p7	4:1111206	TTTACCTGACATCTT[-/CTT]TACCTCCTTCAACAA	285498
rs372487517	snp	G/T			intron-variant	RNF212	GRCh38.p7	4:1103764	AACCTTAGCAAAAAC[G/T]TGATGCACATATAAT	285498
rs372657842	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1095333	ACAGAACCAAGCACA[A/C]CTCCCACAGCTCCAT	285498
rs372750342	in-del	-/AAG			intron-variant	RNF212	GRCh38.p7	4:1060112	CAAAAAAAAAAAAAA[-/AAG]AAAAAAGAAATTGTT	285498
rs372777697	snp	A/C			intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1111835	ATCTGCAAACAACCC[A/C]AAGGGCCATGGACAG	285498
rs372810711	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1108852	CCACAGACGTGTGCC[A/G]CCACAGCCAGATAAT	285498
rs372843539	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1102913	TTGGGAGGCCGAGGC[A/G]GGTGGATCACGAGGT	285498
rs372888744	snp	C/G	0.000164734	0.00907413	missense, synonymous-codon, intron-variant, downstream-variant-500B, nc-transcript-variant	RNF212	GRCh38.p7	4:1073127	GAAATGACACACTCT[C/G]CGGGCACAGGGGGCT	285498
rs372890918	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1107120	GCAGTGGTGTGATCT[C/T]AGCTCACCACAGCCT	285498
rs372901343	snp	C/T	0.0225045	0.103662	intron-variant	RNF212	GRCh38.p7	4:1095260	GCACCTGGCTCATCA[C/T]GGAACCAAGCACACC	285498
rs372944744	snp	C/T	8.24518e-05	0.00642021	intron-variant	RNF212	GRCh38.p7	4:1096884	ATTGTGTCTAATAAA[C/T]GCTTCTGGCCCCCAG	285498
rs372946674	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1091790	AGGGATGACAGCCTC[A/G]CGGTTTCCTGGCTGC	285498
rs372950668	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1058620	GTCTTCCACATGAGG[A/G]CGTAAATATCCTACA	285498
rs372968790	snp	C/T	0.000153988	0.00877328	intron-variant	RNF212	GRCh38.p7	4:1085845	CAGACGACCAATGCA[C/T]ATGGCAGTGGGTGCC	285498
rs373007256	snp	C/T	0.000284241	0.011918	intron-variant	RNF212	GRCh38.p7	4:1085995	TTATCAGACAGGCTA[C/T]GCTGAGTGACATGTG	285498
rs373089666	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1102164	AAGAACAAACTAAAT[C/T]CAGACAAAAAGGAAA	285498
rs373160396	multinucleotide-polymorphism	AC/GT	0	0	intron-variant	RNF212	GRCh38.p7	4:1057062	ATCTCTGGTGACACG[AC/GT]AGTTACAGCACTGGC	285498
rs373195454	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1103316	TGAATGCTACCAAAC[A/G]TTTAAAGAAATAACC	285498
rs373243869	snp	A/G	0.000182945	0.00956238	intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1113344	TCCAGCCTGCGTTCG[A/G]GAAGCCCTGACCTTT	285498
rs373273310	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1111173	TCACTGGGATGTCCA[C/G]TTCATCAACATCTCT	285498
rs373317673	snp	C/T			intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1092892	GGCGGCTGCCTGGTC[C/T]GGAGCACACTTCTCA	285498
rs373393189	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1100386	GTTACATTTCCACAG[C/G]CATTTTCCATAATTT	285498
rs373427911	snp	C/T	0.000399281	0.0141238	intron-variant, missense	RNF212	GRCh38.p7	4:1094220	GGCCAACGGTGGGAG[C/T]TGCACTCTTCACGGA	285498
rs373479665	in-del	-/C	0.00953873	0.0683987	intron-variant	RNF212	GRCh38.p7	4:1097697	GCCTTCCCTCACTTT[-/C]CCCAGCCAGGACCAC	285498
rs373518537	snp	A/G	0.00438332	0.0466095	intron-variant	RNF212	GRCh38.p7	4:1092705	AGGGCTGCGATGGTC[A/G]CAGAGGCTGCGCTGG	285498
rs373524851	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1074195	ACCCAGAGCTGCCAG[C/T]GCAGGTTCTGAGACT	285498
rs373528969	snp	C/T	0.00517822	0.0506191	intron-variant	RNF212	GRCh38.p7	4:1097561	AGTGAGCCGAGATTA[C/T]GCCACTGCACTCCAG	285498
rs373536974	snp	C/T	0	0	intron-variant	RNF212	GRCh38.p7	4:1057424	TAAATATGCAGCAGA[C/T]GGAGTGGGAGGCCAC	285498
rs373544321	snp	C/G	0.00597247	0.0543191	intron-variant	RNF212	GRCh38.p7	4:1079133	CACAGGACCAACATA[C/G]GACCAACACAGGGTC	285498
rs373551967	snp	C/G	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1065682	TCTGGAACTCCTAGG[C/G]TCAGCTCCACCTCGG	285498
rs373656791	snp	G/T			intron-variant	RNF212	GRCh38.p7	4:1090881	GACACAGATCCACGG[G/T]CTCTGTGGCTGGAGT	285498
rs373781736	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1091403	AAGAGAGTCCTGTGA[C/T]TTCCTCAGAGGAAGA	285498
rs373800172	snp	A/C	1.64961e-05	0.00287189	intron-variant	RNF212	GRCh38.p7	4:1081413	TTCTGCAAGCAACCC[A/C]CACACCTGTCGGGGG	285498
rs373888316	snp	C/T			upstream-variant-2KB, nc-transcript-variant, intron-variant	RNF212, TMED11P, LOC105374344	GRCh38.p7	4:1115244	ATGCAGATTATTTGT[C/T]CTTATTGATAATATT	285498
rs373900154	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1068952	ATGGCTCACACCTGC[A/C]ATCCTAGCACTTTGG	285498
rs373913375	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1106850	TATCTTTTGCCCTTG[A/C]TTTTTCATTACTTCA	285498
rs373929804	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1091127	GGGTGCTGTCCCTCT[A/G]ATAATGGCTACTGGT	285498
rs374004263	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1098723	CCTCGGTCTCCCTAC[A/G]TATAAAACAGAAGCA	285498
rs374030388	in-del	-/TG/TGCTG/TGCTGCAGTGGGATAA/TGCTGCAGTGGGATAACCT	0.000923468	0.0214719	intron-variant, utr-variant-3-prime	RNF212	GRCh38.p7	4:1094052	AGAAGCAAGGAAGCT[lengthTooLong]CCCAGAGGAGGACAG	285498
rs374045222	snp	A/G	6.63625e-05	0.00575993	intron-variant	RNF212	GRCh38.p7	4:1090866	TAGGTTTCAGCTGCT[A/G]ACACAGATCCACGGT	285498
rs374130399	snp	C/T			utr-variant-3-prime, intron-variant	RNF212	GRCh38.p7	4:1072054	GGATGAACTATGATA[C/T]ATCCAGATAATGGAA	285498
rs374134594	snp	A/T	0.000148816	0.00862471	missense, utr-variant-5-prime, intron-variant, nc-transcript-variant	RNF212	GRCh38.p7	4:1108344	ACATTTCAACTTACA[A/T]GCTTTGAAAGCAAAA	285498
rs374146978	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1088439	GCATACAGTCACATA[C/T]GTGTTCACAAAGAGA	285498
rs374157508	in-del	-/AC			intron-variant	RNF212	GRCh38.p7	4:1110276	AGGAAAAAATGCAAA[-/AC]CAGCCAATAAACACA	285498
rs374282658	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1077584	TACTCAGATCCTAAG[A/G]AAAGGTAGAAAGCTG	285498
rs374290344	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1096638	CAAGCACACCCCTCA[C/T]AGCTCCATGGTCTCG	285498
rs374307132	snp	A/C/G	0.000366789	0.013538	intron-variant	RNF212	GRCh38.p7	4:1085877	CGACTGCGCACTCAC[A/C/G]GGGGGTGGGGCGCCT	285498
rs374309005	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1085182	GTAGAATCTAAGGCA[C/T]TGCTGAGCGTAATAT	285498
rs374403252	snp	C/T	0.000131861	0.00811869	intron-variant	RNF212	GRCh38.p7	4:1096751	GGAACCAAGCCACAC[C/T]CCTCACAGCTCACCT	285498
rs374447398	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1081160	GGCACGCAGAACACT[A/G]GGTCACATGATCATT	285498
rs374462568	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1063047	AATACCGTTGAAAGA[A/G]ATCAAAGACCTAAAT	285498
rs374564704	snp	C/T			intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1112705	CCCTCATCTTGCATC[C/T]CGCTCCCCCCGGCGG	285498
rs374578346	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1059352	AAGGAAAGCTGTCTT[A/G]CTAGGCTGTGTGAGT	285498
rs374588813	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1095186	TGGTCTCGGGATAGC[A/G]CACCTGGCTCATCAC	285498
rs374611459	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1102804	TTGCAGTGAGCCAAG[A/G]CTGCGCCACTGCACT	285498
rs374626919	snp	A/T			intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1056807	CACTTTCCCAAGAGC[A/T]TTTTCTTCCTGAGGC	285498
rs374753687	snp	A/G	0.000491421	0.0156675	intron-variant	RNF212	GRCh38.p7	4:1073707	AAATTCCAATATTGC[A/G]GCTTACGAGATTCGG	285498
rs374794288	snp	A/T			intron-variant	RNF212	GRCh38.p7	4:1064600	TTTGTGTGTGTGCAG[A/T]GTTAGTAAGCAAGCT	285498
rs374807041	snp	G/T	0.00438332	0.0466095	intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1111758	ACCCAACAGAAATGT[G/T]TACCTAAGATCACCG	285498
rs374809429	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF212, TMED11P, LOC105374344	GRCh38.p7	4:1115189	ATCATAAAAATAATA[A/C]ACATATATGCAGGTA	285498
rs374861387	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1070771	GCTAGGGCACCACAT[C/T]GGTAACATGCTCAGT	285498
rs374876807	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1095289	CCCCCCACAGCTCCA[C/T]GGTCTCGGGATAGCG	285498
rs374926346	in-del	-/ACACACACACACAC			intron-variant	RNF212	GRCh38.p7	4:1106250	TAAACAATTTTACTT[-/ACACACACACACAC]ACACACACACACACA	285498
rs374968061	snp	C/T	0.00478085	0.0486577	intron-variant	RNF212	GRCh38.p7	4:1109038	TTTGAGACAGAGTTT[C/T]ACTCTGTCACCCAGG	285498
rs375103536	snp	A/G	1.73918e-05	0.00294883	intron-variant	RNF212	GRCh38.p7	4:1081636	TAAATAGATGGAGAA[A/G]AGGTATTGAATTAAA	285498
rs375249286	snp	A/G			synonymous-codon, upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant	RNF212, LOC105374344	GRCh38.p7	4:1113384	GGCGTCGCAGTACAC[A/G]TGCCCGCAGTTGGTG	285498
rs375273481	snp	C/T	0.00438332	0.0466095	intron-variant	RNF212	GRCh38.p7	4:1110531	CGGCAGAAACTATGT[C/T]ATGGTATGATAGCCA	285498
rs375321823	snp	C/G/T	8.24825e-05	0.0064215	missense, utr-variant-3-prime, nc-transcript-variant	RNF212	GRCh38.p7	4:1073604	TTTTACTTACCCATT[C/G/T]GTCCATCTTGAGGTG	285498
rs375369624	snp	C/G	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1107088	ACTGAGTCTTGCTCT[C/G]TCGCCCAGGCTGGAG	285498
rs375401318	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1092089	GTGCCTGTGTGGGAA[A/G]CTTCTCCAAAGCACC	285498
rs375409179	snp	A/G	0.000153988	0.00877327	missense, upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant	RNF212, LOC105374344	GRCh38.p7	4:1113365	CCTGACCTTTGCCGA[A/G]GCAGGCGTCGCAGTA	285498
rs375431000	snp	C/T	0.000346681	0.0131613	intron-variant	RNF212	GRCh38.p7	4:1081495	TGACGAAAATGCCAG[C/T]GTCAGTGCACACAGT	285498
rs375445210	snp	C/T	1.64746e-05	0.00287002	missense, intron-variant, nc-transcript-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1073035	AGTTGGTGAGTTCCC[C/T]GTGCCTTCCAGAACT	285498
rs375492151	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1110230	GAAAGAAACACCTCA[A/G]TAAAAGGCTATGAGG	285498
rs375492402	snp	G/T			intron-variant	RNF212	GRCh38.p7	4:1075190	TGTACGCATCGGTGT[G/T]TTCACATCTGCATTT	285498
rs375649171	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1065756	CACACCTGGCTAGTT[C/T]TGGCATTTTTAGTAG	285498
rs375691062	snp	A/G	1.65488e-05	0.00287647	intron-variant	RNF212	GRCh38.p7	4:1079631	GGAACTCAGCAGGAG[A/G]GATGCACTTACTTTT	285498
rs375715314	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1083757	GGTGGCCTAAGACGA[C/T]GGAGATCACAGCAGA	285498
rs375717743	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1108257	ACTGAAAATTTTAGA[C/T]ACCACAAATGACTAA	285498
rs375781084	snp	A/G	0.0379877	0.132479	intron-variant	RNF212	GRCh38.p7	4:1096484	CGGTCTCGGGATAGC[A/G]CACCTGGCTCATCAC	285498
rs375917351	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime, intron-variant	RNF212, LOC105374344	GRCh38.p7	4:1113633	CCCGCCAACCTCGCG[A/G]GTTCTCCCGCAGCAC	285498
rs375947137	snp	C/G	3.47132e-05	0.00416598	missense, upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant	RNF212, LOC105374344	GRCh38.p7	4:1113397	ACGTGCCCGCAGTTG[C/G]TGAGGCTGAAGCACG	285498
rs375964086	snp	C/G	0.00119737	0.0244387	intron-variant, utr-variant-3-prime	RNF212	GRCh38.p7	4:1094030	CTGTGGGTGATTCAG[C/G]CTGTTTCAGAAGCAA	285498
rs376000736	snp	C/T	0.00438332	0.0466095	intron-variant	RNF212	GRCh38.p7	4:1066411	TCGACTTACTGCAAC[C/T]TTTGCCCCCCAGGCT	285498
rs376036227	in-del	-/GGACCAACACG			intron-variant	RNF212	GRCh38.p7	4:1078913	CACAGGGTCAACACA[-/GGACCAACACG]GGACCAACACAGGGT	285498
rs376173829	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1096954	GACTCAAGTGGCCAG[C/T]ACATTGTGAATGGCC	285498
rs376252054	snp	A/G			intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1058139	AAACAGGGATGAAAA[A/G]CAACATATTAAATTT	285498
rs376282890	snp	A/G	3.30398e-05	0.00406434	intron-variant	RNF212	GRCh38.p7	4:1090759	CAAAAAAATTCAAGT[A/G]GCAATGAATCAATTC	285498
rs376362289	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1080024	CTCTGCCAACACCTG[C/T]CTGGAGCCTGCTGGA	285498
rs376388130	snp	C/T			upstream-variant-2KB, intron-variant	RNF212, TMED11P, LOC105374344	GRCh38.p7	4:1115145	GTTATAATGATATAA[C/T]GTTAATCTCAATCTC	285498
rs376424627	in-del	-/AT/TT			intron-variant	RNF212	GRCh38.p7	4:1083945	TCCACATTTTGTGCA[-/AT/TT]TTTTTTTTTTTTTTT	285498
rs376476949	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1079188	CACAGGGTCAACACA[A/G]GACCAACATGGGACC	285498
rs376551409	snp	A/G			synonymous-codon, intron-variant, downstream-variant-500B, nc-transcript-variant	RNF212	GRCh38.p7	4:1056887	GATGGGCGGCCGGGG[A/G]GGCAGCCTGGCCTGG	285498
rs376558361	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1111447	AGCTCAGGGGCCCTG[C/T]ACCCCACCCTGCTGT	285498
rs376562788	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1096587	ACTCCCACAGCTCCA[C/T]GGTCTCGGGATAGTG	285498
rs376583633	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1062742	ATAAATAAAAGGCAT[C/T]GTGGTTGGAAAGGAA	285498
rs376596631	snp	A/G	0.00199481	0.0315187	intron-variant	RNF212	GRCh38.p7	4:1107693	CTGATCTCGTGATCC[A/G]CCCATCTTGGCCTCC	285498
rs376647447	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1074205	GCCAGCGCAGGTTCT[C/G]AGACTGGTAAGGGAG	285498
rs376679733	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1096051	GCACACCCCCCACAG[C/T]TCCATGGTCTCGGGA	285498
rs376694614	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1074786	TGAAATCAGGAGCTT[C/T]TGTCTCTGTACCTTC	285498
rs376709037	snp	A/G	0.00159617	0.0282053	intron-variant	RNF212	GRCh38.p7	4:1090079	AAGATGGCCTGAGTG[A/G]TGACAGGATGGGGTA	285498
rs376718640	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1102310	CAGGACCCCAAGTGT[A/G]CTGAAATCCAGGCAT	285498
rs376740925	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1088366	ATGATTTAGGGCATC[C/T]GGCAGAAGAAATTTC	285498
rs376742780	snp	A/T			intron-variant	RNF212	GRCh38.p7	4:1101540	TAATTCTCCAGAATG[A/T]ATAAGTTCTACTGGG	285498
rs376778478	snp	C/T	0.00755907	0.0610114	intron-variant	RNF212	GRCh38.p7	4:1101788	GCGCAAAAATATCTG[C/T]ACATACACCTAAGAA	285498
rs376852126	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1070313	GTTTTGTAGGACTGT[A/G]CTGTGTCAGCGTGGA	285498
rs376855822	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1090930	GGCTGGAGGGACTCT[C/T]AGGAGAGCTCACAGT	285498
rs376897853	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1088222	GAAGTTCAGGCTGAG[C/G]AGGTCTCAGATGGAG	285498
rs376912904	snp	A/C			intron-variant, missense, downstream-variant-500B	RNF212	GRCh38.p7	4:1093540	TGGGCAGAGCCTGTG[A/C]CCTCCACGGCCCATG	285498
rs376980863	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1109953	CTTCTTCAAGTTGCC[C/G]TCATGCTAAAAACAT	285498
rs377050051	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1104562	AGGTGGGGAGAATGA[A/G]TACAGCCAGGTGCCC	285498
rs377091220	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1068654	CCATATTCACCATTC[C/T]CCATGCTCTTCATTC	285498
rs377101268	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1066906	TTTTGCTCTATGTTT[C/T]CTTAAAAGAGTTTTA	285498
rs377123898	snp	A/T	1.65477e-05	0.00287638	synonymous-codon, utr-variant-5-prime, intron-variant, nc-transcript-variant	RNF212	GRCh38.p7	4:1108361	CTTTGAAAGCAAAAC[A/T]GTACGACAAGGAGCT	285498
rs377132792	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1076026	GAGTCATGATTTTAC[C/T]TTTTCAAAAAGATAT	285498
rs377133648	in-del	-/G			intron-variant	RNF212	GRCh38.p7	4:1066601	TCCCAAAGTGATGGG[-/G]ATGACAAGTGTGCAC	285498
rs377191999	snp	G/T	1.65611e-05	0.00287755	intron-variant	RNF212	GRCh38.p7	4:1079693	TCGACTCCAGTCTGT[G/T]AAACACATAGTGAAA	285498
rs377192633	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1102713	AAAAATTAGCCGGGC[A/G]TGGTGGTGGGCCCCT	285498
rs377367499	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1070804	TTCAGAGAAATACCA[A/G]TGATGACAGATTGGG	285498
rs377420981	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1096299	CAGCTCCACGGTCTC[A/G]GGATAGCGCACCTGG	285498
rs377502825	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	TMED11P, LOC105374344, RNF212	GRCh38.p7	4:1115682	TACCATCAGGCAAAG[C/T]GAATATTACCCAATA	285498
rs377524316	snp	A/G	0.0023933	0.0345097	intron-variant	RNF212	GRCh38.p7	4:1102635	AGGCAGGCAGATCAC[A/G]AGGTCAGGAGATCGA	285498
rs377558515	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1098931	CAGAAATGGGAGCAA[C/G]TGAAGAAGCTGTCAC	285498
rs377561738	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1110697	TCTATAGGAAATGCT[C/T]GGAAGGATATACACC	285498
rs377585172	snp	A/G	0.00199481	0.0315187	intron-variant	RNF212	GRCh38.p7	4:1094405	CTGCGTCAGAAGCTG[A/G]GGGTGGGGGAGGCTT	285498
rs377686905	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1079766	GAAATACACACATGA[C/T]GAGATGATGTGTAAA	285498
rs377718039	snp	G/T	3.33372e-05	0.00408258	intron-variant	RNF212	GRCh38.p7	4:1085881	TGCGCACTCACGGGG[G/T]GTGGGGCGCCTTACC	285498
rs377723734	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1094797	CCCAAACCTGAGATT[C/T]TAACGTGTGAATATG	285498
rs377725394	snp	A/T			intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1111728	GAAATCAACAACTCC[A/T]CTCCCAGGTTACACA	285498
rs377760395	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1090526	CCCCAGGTGGCTGAG[A/G]GGATAAGTGTGGCCA	285498
rs377761458	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1075170	CTGCCACATGGGAGG[A/G]GCTGTGTACGCATCG	285498
rs386670454	multinucleotide-polymorphism	AC/GT			intron-variant	RNF212	GRCh38.p7	4:1057061	ATCTCTGGTGACACG[AC/GT]AGTTACAGCACTGGC	285498
rs386670456	multinucleotide-polymorphism	CCA/TCC			cds-indel, nc-transcript-variant	RNF212	GRCh38.p7	4:1058376	CGGGATGCTCGGGGC[CCA/TCC]GGGAGGAGACGCTGC	285498
rs386670458	in-del	CTGTTTATCTCATCCTAA/GTG			intron-variant	RNF212	GRCh38.p7	4:1066054	TAGCCATCCTAATGG[CTGTTTATCTCATCCTAA/GTG]TGAGATACTATCTTG	285498
rs386670459	multinucleotide-polymorphism	ACC/TCA			intron-variant	RNF212	GRCh38.p7	4:1079496	CACAGCCCACCCCTC[ACC/TCA]CCCACGGGACCAGCA	285498
rs386670460	multinucleotide-polymorphism	AA/GC			intron-variant	RNF212	GRCh38.p7	4:1092801	GCGAACTGGGAGGCC[AA/GC]GAAGGCCTGAGAGTC	285498
rs386670461	in-del	ACCT/CTGCCCAGGCTGGAGCCAGCCATCA			intron-variant, cds-indel, downstream-variant-500B	RNF212	GRCh38.p7	4:1093540	TGGGCAGAGCCTGTG[ACCT/CTGCCCAGGCTGGAGCCAGCCATCA]CCACGGCCCATGCCG	285498
rs386670462	in-del	G/TACAAAAAA			intron-variant	RNF212	GRCh38.p7	4:1102571	CCAAAAATACAAAAA[G/TACAAAAAA]AAAACACAAAAAAAC	285498
rs386670463	in-del	CC/TCT			intron-variant	RNF212	GRCh38.p7	4:1105748	ATATAAAGCGTCCTT[CC/TCT]ACCGCAGGTCAGGGT	285498
rs397691247	in-del	-/T			intron-variant	RNF212	GRCh38.p7	4:1105747	ATATAAAGCGTCCTT[-/T]CCACCGCAGGTCAGG	285498
rs397729926	in-del	-/AT			intron-variant, utr-variant-3-prime	RNF212	GRCh38.p7	4:1093382	CATATTGTAACAAAT[-/AT]GCCAATATTTATGTT	285498
rs397735147	in-del	-/C			intron-variant	RNF212	GRCh38.p7	4:1074918	TTTCTGGATCCTTCC[-/C]ATCCGCTAGGATGTC	285498
rs397830569	in-del	-/A			intron-variant	RNF212	GRCh38.p7	4:1069221	TCTCAAAAAAAAAAA[-/A]GAAATCTATGAATCC	285498
rs397880110	in-del	-/T			utr-variant-3-prime, intron-variant	RNF212	GRCh38.p7	4:1072289	CGCACAGAGGATTTT[-/T]AGGGTGTGGCACTAT	285498
rs398063190	in-del	-/AAAC			intron-variant	RNF212	GRCh38.p7	4:1083672	AACAAACAAACAAAC[-/AAAC]TCAGTGGGGTTCACT	285498
rs398092116	in-del	-/G			intron-variant	RNF212	GRCh38.p7	4:1059543	CAACCCCAAGCCTGG[-/G]CGGCCTGTTCCACTC	285498
rs527251559	snp	C/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1066189	CAGCCTCCTGAACAG[C/G]TGGGACTACATGCAT	285498
rs527270868	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1060245	CAGTGCTCAAGAGAG[C/T]CAAGTGTGGGCCATG	285498
rs527294043	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1104748	TGGGGCAGCATGTGG[C/T]CCCTTCCCTCGGGTC	285498
rs527319454	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1091097	GAGTGGTGCTCTACT[C/G]CTGGGCCAATCACAG	285498
rs527337846	snp	C/T	0	0	intron-variant	RNF212	GRCh38.p7	4:1065811	GGCTGGTCTTGAAGT[C/T]CTGACCTCAAGTGAT	285498
rs527367850	snp	A/G	0.000798403	0.0199641	intron-variant, synonymous-codon	RNF212	GRCh38.p7	4:1094258	AAGGAAGTGCAGGGC[A/G]GGGGCCAGGGGAAGG	285498
rs527398728	snp	C/G	0.000399281	0.0141238	downstream-variant-500B	RNF212	GRCh38.p7	4:1055835	CCGGCTGGCGGGAGA[C/G]ACCTGGGCTCTGAGA	285498
rs527429469	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1099469	TGTATGGTGGGGCCT[C/T]CTGCAGTGAGAGCCA	285498
rs527433673	snp	A/G	0.000399281	0.0141238	intron-variant, missense, downstream-variant-500B	RNF212	GRCh38.p7	4:1093789	TCCTGCTGGGATGGA[A/G]CAGGGTGAGGGGGTG	285498
rs527437418	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1089948	TCAGGTTATTCTTTA[C/T]AGCAGTATGAAGACA	285498
rs527448063	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1067928	GAAAGTACAAGGCCT[C/G]TACAGTGAAAATTGC	285498
rs527454997	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1083157	ATCAGCAGAAATATA[C/T]CTCCCTCCAGCGAGA	285498
rs527465998	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1057376	GGACCTTTGAACACA[C/T]GAGTTCGGTTGACAG	285498
rs527499963	snp	G/T	0.00358779	0.0422022	intron-variant	RNF212	GRCh38.p7	4:1066200	ACAGCTGGGACTACA[G/T]GCATGAGCCACTATA	285498
rs527578977	snp	A/G	0.00159617	0.0282053	intron-variant	RNF212	GRCh38.p7	4:1083580	CAGGCGGAGGTTGAG[A/G]TGAGCTGAGATCGTG	285498
rs527603304	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1092550	GCCCAGAGACTTGAG[A/G]CACTGGGTGTGGCCT	285498
rs527689791	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1089849	CCCTTTGCCTTCTGC[C/T]GTGACTGTAAGTTTC	285498
rs527690718	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1059894	GAGGTCGGGAGTTCA[A/C]GACCAGCCCGACCAA	285498
rs527715530	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1078884	GGGTCAACACAGGAC[C/T]GACATGGGACCAACA	285498
rs527789723	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1066972	TTGACTTTTCTACAT[A/G]GTGTTAGGAAGGAGT	285498
rs527804042	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1088101	GGGCAGAAGTTGGAA[C/G]AATTTGGAGGGCTCA	285498
rs527816348	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1105238	TCTAGCTTACACTCT[A/C]CCTCCTCAAGGAGGC	285498
rs527866262	snp	C/T	0.00358779	0.0422022	upstream-variant-2KB, nc-transcript-variant, intron-variant	RNF212, TMED11P, LOC105374344	GRCh38.p7	4:1115268	TAATATTTTAAACAA[C/T]CTTCTTAGCTATAAA	285498
rs527893595	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1100766	TCTCTATCATCATAT[G/T]TGACCACTATGGCTG	285498
rs527893634	in-del	-/TT	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1083983	GACGGAGTTTTGCTC[-/TT]GTTACCCAGGCTGGA	285498
rs527921562	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1061121	AGCTTTGGGAGGAGC[A/G]GGACTTGGCTTCCCA	285498
rs527928599	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1067674	GATCGAGGCCAGCCT[C/T]GTCAACATGGTGAAC	285498
rs527932789	snp	C/T	0.0479392	0.147212	intron-variant, utr-variant-5-prime	RNF212	GRCh38.p7	4:1099811	GAGCAATCGAGTCCA[C/T]AAGGTCCGACGGCGC	285498
rs527977205	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1095842	GGGATAGCGCACCTG[A/G]CTCATCACAGAACCA	285498
rs528149645	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1107942	TGAATATTTTATAGA[A/G]AGAACAAAAGGCATT	285498
rs528170345	snp	A/G	0.00159617	0.0282053	intron-variant	RNF212	GRCh38.p7	4:1102611	AAAAAAAAACACTTT[A/G]GGAGGCTGAGGCAGG	285498
rs528183446	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1070013	CTGTGTCAGCGTGGA[C/T]GCCTGGCCTGAGTTA	285498
rs528189057	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1076688	CTACACACATCCACT[C/T]CAGGGTGACAAGGCG	285498
rs528242940	in-del	-/A	0.301177	0.244706	intron-variant	RNF212	GRCh38.p7	4:1102989	CTACTAAAAAAATAC[-/A]AAAAAAAAAAAAATC	285498
rs528285284	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1102943	TCAGGAGATCGAGAC[C/T]ATCCTGGCTAACAGG	285498
rs528305735	snp	C/T	0.0134861	0.0810011	intron-variant	RNF212	GRCh38.p7	4:1070557	GCCTGGCCTGAGTTA[C/T]AGGTGGTTTTGTAGG	285498
rs528307703	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1102838	GCCTAGGCAACAGAG[A/C]GAGACTCCGTCTCAA	285498
rs528377653	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1059105	AGCATTAGGCTTCCC[C/T]AGCGCAGTGACTGTG	285498
rs528378467	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1097930	GTTACCTGGGCGTGA[C/T]GGCAGGTGCCTGTAA	285498
rs528433123	snp	G/T	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1088210	GATATGGATGGTGAA[G/T]TTCAGGCTGAGGAGG	285498
rs528573112	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1082103	CACTCCTGCTTGGGT[A/G]ACAGAGCAAGAACTC	285498
rs528630581	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1077888	CAGCTCCCGTGTTGC[A/C]GGTGGGTGTGGGCGT	285498
rs528690813	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1077373	CTAGTGAAGTGTCAA[C/T]CAATTTAGCCTGCCA	285498
rs528691994	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TMED11P, LOC105374344, RNF212	GRCh38.p7	4:1115658	GACCTATTCGTATAT[G/T]TTATTTGCTACCATC	285498
rs528709157	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1061356	CGAGGGGTCCATCTG[C/T]AGGACCTGGAGAGGC	285498
rs528721181	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1082074	TGAGCTGTGATTGTA[C/T]TACTGTACTACTGCA	285498
rs528749599	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1104269	ACATGCGAAGATGAA[A/T]GTAGGCCAACTGGTG	285498
rs528766201	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF212	GRCh38.p7	4:1072128	GAGATGGGGGAACCA[C/T]AAGTGTGTATTGCTA	285498
rs528777320	snp	G/T			intron-variant	RNF212	GRCh38.p7	4:1105548	TTTTACATGGTAGTG[G/T]CTGTCACAATCAGGT	285498
rs528812722	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1102870	AAAAAGGCCGGGCAC[A/G]GTGGCTCACACCTGT	285498
rs528840240	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1057302	ACTGCAGGCATCAAA[A/C]GCCACTCAAGGGCTC	285498
rs529008777	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1079925	AGGCCGCTGGCCGGC[C/T]CGCCCTGGTTGGGCT	285498
rs529034268	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1090638	AGGAGACAGTGACAA[C/T]GTCCCCATAGCTGGA	285498
rs529037558	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1074175	CAACCCACAGGAACC[C/T]GTGAACCCAGAGCTG	285498
rs529059190	in-del	-/AG			intron-variant	RNF212	GRCh38.p7	4:1066513	TTTAAGTTTTTTTGT[-/AG]AGATGGGGGTTTCAC	285498
rs529070295	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1084668	CTTGGGAGGTTGAGG[C/T]GTGAGCTGAGATCAC	285498
rs529075508	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1111568	CGACTCATGTCTGCT[C/G]AATCTACCTAACTTC	285498
rs529105560	in-del	-/C	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1112688	GCCCGACCCCTGTGT[-/C]CCCCTCATCTTGCAT	285498
rs529106355	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1104758	TGTGGCCCCTTCCCT[C/T]GGGTCCCGATTTGGC	285498
rs529183911	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1074897	CTGGAGTGCTGCTAT[A/G]CCATCATTTCTGGAT	285498
rs529224326	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1111950	ATACAATGATAAACT[G/T]TGCTAATCCCACATT	285498
rs529242746	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1069098	TGCCTATAGTCCCAG[C/T]TACTTGGGAGACTGA	285498
rs529260075	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1101451	ATGGTATTCCCTTCT[A/G]CTTAAGATGGGATTT	285498
rs529273545	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1062293	TACACCACGACCAAC[C/T]GGGATTCATCTCAGG	285498
rs529282380	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1106889	TGCCACAGAAATATT[C/T]TTATAAGTGTGGAGA	285498
rs529321339	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1106011	GCATGGGGGACTTTG[A/G]CGCTTACTCCTGGAA	285498
rs529322218	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1068420	GATTTTTCAGCTGTG[G/T]TTTTAGAGTTATGTT	285498
rs529331246	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1082355	GGCCTGGTGGACATG[A/C]TGAGATGCACACGTA	285498
rs529331930	snp	C/T	0.0689305	0.172377	intron-variant	RNF212	GRCh38.p7	4:1096515	GGAACCAAGCACACC[C/T]CCCACAGCTCCACGG	285498
rs529378072	in-del	-/C	0.0221141	0.102801	intron-variant	RNF212	GRCh38.p7	4:1083647	TGTCTCAAAAACAAA[-/C]AAACAAACAAACAAA	285498
rs529414294	snp	A/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1057863	TGAGGTCGGGAGTTC[A/G]AGACCAGCCTGACCA	285498
rs529414377	snp	C/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1062761	GTTGGAAAGGAAAAA[C/G]TAAAACAACCTCCAC	285498
rs529510471	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1091923	GCTATGAAGAGGAGT[A/G]GACAGAAGGACTCCG	285498
rs529536619	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1064686	ACCATTTTCAGTGTA[C/T]AGTTCACTGGTATTA	285498
rs529631028	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1103794	TACTTGATGAAATAC[C/T]GGAAGCTTGACCCTG	285498
rs529641679	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1109167	TGCCTGCCACCACAC[A/C]AGGCTAATTTTTGTA	285498
rs529691252	snp	A/T	0.000399281	0.0141238	downstream-variant-500B, intron-variant	RNF212	GRCh38.p7	4:1071261	CAAAATAAATTATTT[A/T]AAAAAAACTAACTTG	285498
rs529741439	snp	G/T			utr-variant-3-prime, intron-variant	RNF212	GRCh38.p7	4:1072456	TTTAACACATGGACT[G/T]CTCTGGTGGAGGATG	285498
rs529765298	snp	C/T	0.00159617	0.0282053	intron-variant	RNF212	GRCh38.p7	4:1104215	CAACAGGATTCTGTG[C/T]CTGTGGAAATTGACG	285498
rs529765397	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1099930	CAGGAAAGGGGCGCT[A/G]CAAAAGAGGGCTCTT	285498
rs529774372	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1058875	GAGCATCTGGAGCAC[A/G]AGCTTCCTCCCCCGC	285498
rs529825825	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1059759	TAATAACGATGGCAG[A/G]TATCTTTTGTTAAGT	285498
rs529962814	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1060180	ATTATCAACAGAGAT[A/G]AAGAGACTGAGGACC	285498
rs529980591	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1089367	TTGTTTTGGTCAATT[C/T]CTCCCATTTGGAATG	285498
rs529985048	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1088969	GAAGTCTGCTGCAGA[A/G]GCAGAGCCCTCATGG	285498
rs529996267	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1082727	GAGGACGGGCACTGG[A/G]CGTGTTTGGCTTACT	285498
rs530023453	snp	G/T	0.000399281	0.0141238	downstream-variant-500B	RNF212	GRCh38.p7	4:1056165	GAACTCAACAGGCAG[G/T]TGTTCGTTTTGCCTC	285498
rs530214773	snp	A/C	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1078851	GGACCAACACAGGAC[A/C]AACATAGGACCAACA	285498
rs530217644	snp	A/G/T	0.0174175	0.0916809	utr-variant-3-prime, intron-variant	RNF212	GRCh38.p7	4:1071587	CTTAAAACTCAACAA[A/G/T]AAGAAAACAATCCAA	285498
rs530232590	snp	G/T			intron-variant	RNF212	GRCh38.p7	4:1098383	GATTAAGGCACCAGC[G/T]CCAAAGCCTGGGGCA	285498
rs530262836	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1066396	TGCAGTGGCACAATC[C/T]CGACTTACTGCAACC	285498
rs530295559	snp	C/T	0.00636936	0.0560724	intron-variant	RNF212	GRCh38.p7	4:1095098	CGGAACCAAGCACAC[C/T]CCCCACAGCTCCATG	285498
rs530307340	snp	C/T	0.00159617	0.0282053	intron-variant	RNF212	GRCh38.p7	4:1105162	ACTGTGGGGCATCCT[C/T]GTCCTTCACCTCCTT	285498
rs530339242	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1061101	GACTCCTGAAATCCC[A/G]TTGCAGCTTTGGGAG	285498
rs530345389	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1111749	AGGTTACACACCCAA[C/T]AGAAATGTGTACCTA	285498
rs530353564	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1073490	CACCGGGTGGAAGGA[C/T]AGCACCCCCTTGGGT	285498
rs530382504	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1100691	TGGGATTACAGGCGT[A/G]AGCCACCGCACCCGG	285498
rs530475339	snp	A/G	0.000148212	0.00860722	utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant	RNF212, LOC105374344	GRCh38.p7	4:1113506	GCCGGGCCCACGCGA[A/G]GCCCACGCAAGGTTG	285498
rs530476206	snp	C/T	0.0111196	0.0737302	intron-variant	RNF212	GRCh38.p7	4:1080578	GTCACAGCGGGACCC[C/T]GTGGAGCTTGTGCCT	285498
rs530533480	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1085590	ACCCCACCTGTGCTG[A/G]GTCACTCTGAGAGGC	285498
rs530570974	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1107021	CCTTTTAAGAGTGAG[C/T]GTGCCCAAAATATAA	285498
rs530610050	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1080971	AGCCACAGGACATGT[A/G]CCAGTATGAACGTTT	285498
rs530654746	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1069304	AGCTCTTCTTTATAG[C/T]AGAATGACAATTAAT	285498
rs530713739	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1102100	TTATGACCCTATAGT[A/G]TAATATTACAGAGGA	285498
rs530725450	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1063590	CCTGTAATCCCAGCT[C/T]GTCAGGAGGCTGAGG	285498
rs530792801	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1059040	TGAGTTCTCAAGCAA[C/T]ACCTGCTCCTGGACC	285498
rs530794013	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1102897	CTGTAATCCCAGCAC[C/T]TTGGGAGGCCGAGGC	285498
rs530801684	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1096984	CTCTCAGGGGCCCTG[C/T]CAGGGACAGCCTCGA	285498
rs530811722	snp	A/C	0.00478085	0.0486577	intron-variant	RNF212	GRCh38.p7	4:1097460	ATATAAAAAAATTAG[A/C]CGGGCGTGGTGACGG	285498
rs530853205	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1064200	AGATTTATAACACAT[A/T]GATCCCATATATATG	285498
rs530946717	snp	G/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1092830	GTCAAGGCAGTCGGG[G/T]GAGAATGCAGGTCAC	285498
rs530963548	snp	C/G/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1082085	TGTACTACTGTACTA[C/G/T]TGCACTCCTGCTTGG	285498
rs530981635	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1058754	CCCAGCTGAGTTTCA[G/T]CCTCACTGAGGGGCC	285498
rs531049714	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1079939	CCCGCCCTGGTTGGG[A/C]TCTCCCTGGCATTCC	285498
rs531108521	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1077289	GCCCATGTCTGGTCT[C/T]TGCCCCTCACTTAGG	285498
rs531109461	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF212, LOC105374344	GRCh38.p7	4:1114319	TTATAAAATTGTCCT[C/T]TGCGTGGTTTTGAGA	285498
rs531124051	snp	C/T	0.00199481	0.0315187	upstream-variant-2KB, intron-variant	RNF212, TMED11P, LOC105374344	GRCh38.p7	4:1115020	CTGTGGTGAGCCTGA[C/T]GGCACCTGTGCAGCA	285498
rs531188425	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	RNF212	GRCh38.p7	4:1056351	TACACATGCTGGTGG[A/G]CACGAAGGCTGGAGG	285498
rs531210551	snp	G/T	0.00597247	0.0543191	intron-variant	RNF212	GRCh38.p7	4:1094432	GCTTGGAGTGGAGGC[G/T]CGTGCTGACTGGGAG	285498
rs531246722	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1060731	GTGATGCCAGATCCA[C/T]TGTGCTGTGTTCTGG	285498
rs531313184	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1061056	AGACAACAAATCAGA[A/C]AACATTGACTCCTGA	285498
rs531342421	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1089526	GTTTATGCGGGAATG[A/G]GTTAAAACTTTGGGG	285498
rs531354829	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1084069	TTCTCCTGCCTCAGC[C/T]TCCTGAATAGCTGGG	285498
rs531386414	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1092779	ACGCGTGCTTTGCCC[A/G]CATCCTGCGAACTGG	285498
rs531388248	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1111303	TATCTAGGATTATAG[A/G]ATTATTATCCCGTAT	285498
rs531453338	snp	C/T	0.000399281	0.0141238	missense, intron-variant, downstream-variant-500B, nc-transcript-variant	RNF212	GRCh38.p7	4:1056843	GAGCACTTGCCTAAA[C/T]ACTGCCTCTGCAGCA	285498
rs531505537	snp	C/G	0.000429121	0.0146416	missense, utr-variant-3-prime, nc-transcript-variant	RNF212	GRCh38.p7	4:1073644	TGGAGATTCTCGCAG[C/G]GCCGGCTGCTATCTC	285498
rs531634569	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1079397	GCCAACACCTCGTCC[C/G]CATTTGCTTTTGTTT	285498
rs531682645	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1092333	GAAAGTCTCCAAGGG[A/G]ACCTGAGCAGCAGAT	285498
rs531798811	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1101427	ATCGTTCTGAAAGGT[C/T]CTGTAAACATGGTAT	285498
rs531843561	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1068353	CTTTGTCCTTCTATT[G/T]TCTTGATTGTCTTTA	285498
rs531845459	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1061687	ACAGGCGGACACCCC[A/G]GGACATCTCAGCTCA	285498
rs531926020	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1058224	AATTTCCTTTAAAAC[A/G]CTGTGAAGAAGGTGC	285498
rs531935415	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1095893	ATGGTCTCAGCATAG[C/T]GCACCTGGCTCATCA	285498
rs531973260	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1108079	CCTGTATTGTGCTGC[A/G]GAAATCTATTTAACC	285498
rs531994599	snp	A/C	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1102427	TGTATTTTTGATCTG[A/C]ATCTGACTGGAAAAA	285498
rs532021374	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1091793	GATGACAGCCTCGCG[A/G]TTTCCTGGCTGCTGC	285498
rs532105152	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1098498	GTGAGCTCCTCTGTA[A/G]CAGGGGGACTGAGAC	285498
rs532248110	snp	A/T	0.000399281	0.0141238	downstream-variant-500B, intron-variant	RNF212	GRCh38.p7	4:1071103	CAAAATAAATTATTT[A/T]AAAAAACTAATTTGT	285498
rs532299625	in-del	-/CCTATCACAGGGG	0.00159617	0.0282053	intron-variant	RNF212	GRCh38.p7	4:1080798	AATCTGAATGTGTTT[-/CCTATCACAGGGG]TGGACTGAATTTGTG	285498
rs532373791	snp	C/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1059136	ACTGGCCAGTGCCCT[C/G]CCTGCTGCGGCACGT	285498
rs532434311	snp	A/G	0.000151573	0.00870421	intron-variant, synonymous-codon, downstream-variant-500B	RNF212	GRCh38.p7	4:1093682	AAACCACCCTGGAGC[A/G]CACGGCCTGTGGCTC	285498
rs532434397	snp	C/G/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1088425	TGGCTTTTTCTGAAG[C/G/T]ATACAGTCACATACG	285498
rs532514485	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TMED11P, LOC105374344, RNF212	GRCh38.p7	4:1115737	CAGCCTTTATGCCAG[A/G]CATTAGGCCAAGCAC	285498
rs532533474	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1065915	AGGATCTTACTCTGT[C/T]GTCCAGGCTGGAGTG	285498
rs532563577	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1082247	GCAACCCTGGACTGA[C/T]CTCCACGATGGCCAG	285498
rs532594230	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1062467	ATTTAACCCTTCTTC[A/G]TGACAAAAAAGGACT	285498
rs532659346	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1099530	CAGGAGAAGGGGGAT[C/G]GGTGAGAGCTGAGGC	285498
rs532768353	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1078374	TGCCTCCTCTCTCCC[A/G]TTTCCGAGCTGCCTG	285498
rs532776740	snp	C/T	0.0023933	0.0345097	intron-variant	RNF212	GRCh38.p7	4:1111401	CTTCCCCTGGATGGC[C/T]CTCACAGGATACAGG	285498
rs532900941	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1084951	ACCAGCCAGTGTGAC[C/T]GGCGTCACCAGCTTC	285498
rs532927721	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1075397	TGCTTCTGGGGAGGC[C/T]TTGGGAGGCTACAAT	285498
rs532978933	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1106428	CTCATCAGAATGCCA[C/T]AGGACTAAAAATTAA	285498
rs532988017	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1074938	GCTAGGATGTCTTCA[A/G]TATCAAGTTCATCCT	285498
rs532989447	snp	A/T			intron-variant	RNF212	GRCh38.p7	4:1092629	GAGTGTTTATCTTGC[A/T]GAGAATATGCCTCTT	285498
rs532998167	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1092494	CTGCAGCCTCATGCC[A/G]CCTCCGTGGTTTGTC	285498
rs533013632	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1080488	CTGTGGGAGGGTGGA[C/T]AAAACCCACTTGGCT	285498
rs533020238	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1091046	TAATGGGCATGATAG[A/G]AAAGTCTCCCCAGCA	285498
rs533165688	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1096615	GTGCACCTGGCTCAT[A/C]ACAGAACCAAGCACA	285498
rs533279828	snp	A/T			intron-variant	RNF212	GRCh38.p7	4:1100934	AGATACAGATGTGTT[A/T]TAGCTGTTCAGATGG	285498
rs533289958	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1106949	TTGTTTGAAACAGCG[A/G]AAAACCGAAAAAATC	285498
rs533298860	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1096969	CACATTGTGAATGGC[C/T]TCTCAGGGGCCCTGC	285498
rs533310511	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1087565	CTGACAGGACAGGGT[A/G]GGTGTGACAGGAGCA	285498
rs533415701	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1084492	TGCAGCACTTTGGGA[C/T]GCTGAGGTGGGAGGA	285498
rs533456660	snp	A/G	1.66471e-05	0.00288501	missense, intron-variant, nc-transcript-variant	RNF212	GRCh38.p7	4:1081599	ATTGTGCTGAAAGCT[A/G]TTTGTTGTGATGATC	285498
rs533463640	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime, intron-variant	RNF212, LOC105374344	GRCh38.p7	4:1113638	CAACCTCGCGGGTTC[G/T]CCCGCAGCACCTGGG	285498
rs533576001	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1066763	TGCCTTTTTACTCTA[C/T]TGATAGTATCTTTTG	285498
rs533635351	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1082470	TGCCCGTCTATGCTG[A/G]CTGGGTTTTGAGATA	285498
rs533881409	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1090068	GTGGTGGTAGCAAGA[C/T]GGCCTGAGTGGTGAC	285498
rs533968485	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1066008	TGTTCCAAGTAGCTA[C/G]GACTACAGGTGCGAT	285498
rs533992829	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1077679	GAAACAAGGCCCTAG[C/T]GCAGCAAGGGACAGC	285498
rs534012760	snp	A/G	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1082809	AACACTGGCTGCTGC[A/G]TGGCTGACTGTGGTG	285498
rs534020879	snp	A/T	0.00438332	0.0466095	intron-variant	RNF212	GRCh38.p7	4:1106026	GCGCTTACTCCTGGA[A/T]AGTTGGGATGCATTT	285498
rs534063901	snp	C/G	0.00398564	0.0444627	intron-variant	RNF212	GRCh38.p7	4:1084096	TGGGATTACAGGTGT[C/G]CACCAACACATCTGG	285498
rs534071689	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, intron-variant	RNF212	GRCh38.p7	4:1072493	ATGGGGGAGCTGTGC[A/G]TGTGTGGAGTCATGG	285498
rs534087400	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1063995	TGAAATTATCCTTCA[A/G]AATGAAGACAAAGAC	285498
rs534140813	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1089690	TCAAGGGAGGGATCC[A/G]GTGGGAAGTGATTGG	285498
rs534161196	snp	C/G	0.00159617	0.0282053	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	RNF212	GRCh38.p7	4:1056489	TTGTCTTTGAAATGA[C/G]TTCAAAACTTCACAC	285498
rs534213507	snp	A/C/T	9.88361e-05	0.00702917	missense, intron-variant, nc-transcript-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1073083	GCCAGTGAGGACAGA[A/C/T]GTCTATGCAGAAACA	285498
rs534235347	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1074132	TCTATCCAGCAACCA[C/T]GAGGCCGCTTCTGCC	285498
rs534273210	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1083472	ACATGGTGAAGCCCC[A/G]TCTCTACTAAAAATA	285498
rs534290662	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1069459	GACACTCATCCATTA[C/T]GGGGGACATAGTGGC	285498
rs534482239	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1058777	GAGGGGCCCTCGGCC[C/T]GTGGGCTCTGCGAGG	285498
rs534541270	snp	C/T	0.000399281	0.0141238	missense, nc-transcript-variant	RNF212	GRCh38.p7	4:1058388	GGCCCAGGGAGGAGA[C/T]GCTGCCTGTGGTGGA	285498
rs534578464	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1062602	GAACAAAGACAAGGA[C/T]GTCTGTTCTTGCCGC	285498
rs534598346	snp	A/G	0.0023933	0.0345097	intron-variant	RNF212	GRCh38.p7	4:1086448	TTGCTGGGAGGATTA[A/G]GAGACAACATACACA	285498
rs534635568	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1075627	ATTCCACATGAGATT[C/T]GGGCAGGGACAAATA	285498
rs534645212	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1068797	TTTAGTCTTCATTTT[A/G]AAATGTTAATTTCAT	285498
rs534655003	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1076502	GTGGGAGGTTCACCT[C/G]GAGAGAGGCCTGCAC	285498
rs534658543	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1081758	CATTTCACATGAATT[C/T]AGCAGTTCCCATAGC	285498
rs534674839	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1096716	TCCATGGTCTCGGGA[G/T]AGTGCACCTGGCTCA	285498
rs534729897	snp	C/G/T			intron-variant	RNF212	GRCh38.p7	4:1078068	GGTCCCTCCATCATC[C/G/T]GGCTCCGGGTGTGAT	285498
rs534746617	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1102214	AATAGGAAACAAATA[C/T]AAAATGGACACGATC	285498
rs534786405	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1076992	CCCAGCACTTTGGGA[C/T]GCTGAGGTGGGCAGA	285498
rs534805223	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1095997	ACTCCCACAGCTCCA[C/T]GGTCTCGGGATAGCG	285498
rs534818618	snp	A/G	0.00398564	0.0444627	intron-variant	RNF212	GRCh38.p7	4:1097037	TGGCCACTTCCCTCT[A/G]AGGGCTGTGCCGGAC	285498
rs534853284	snp	A/T			intron-variant	RNF212	GRCh38.p7	4:1085069	CTCACCCACCCCTAC[A/T]CACACAGCCAATGGG	285498
rs534874281	snp	C/T	0.00398564	0.0444627	intron-variant	RNF212	GRCh38.p7	4:1107306	TCCGCCTGCCTCAGC[C/T]TCCCAAAGTGCTGGG	285498
rs534901014	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1103222	GAACTTTAAACAGTT[C/T]GATGTCTAATAAAGA	285498
rs534913683	snp	A/T			intron-variant	RNF212	GRCh38.p7	4:1101217	GTGCAGTAGCCGTGG[A/T]GGCATCTCTACACAC	285498
rs534959965	snp	A/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1093075	GAGGATTACTGGGAA[A/G]AGGAAGATGTTTAAT	285498
rs534964140	snp	G/T	1.66829e-05	0.00288811	intron-variant	RNF212	GRCh38.p7	4:1085857	GCACATGGCAGTGGG[G/T]GCCTCGACTGCGCAC	285498
rs534997992	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	RNF212, LOC105374344	GRCh38.p7	4:1113894	GCCCACCTTGAGGGC[C/T]GGGAGCTGGGCCGGA	285498
rs535020251	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1097678	TCACCTCCCTGCACC[C/T]CTGGCCTTCCCTCAC	285498
rs535100738	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1083312	GGTGAAATGAGCAGG[A/T]ATGTTCTCAAAATGT	285498
rs535108363	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1101415	AAACTCTGGCTCATC[A/G]TTCTGAAAGGTCCTG	285498
rs535109099	snp	C/T	0.00636936	0.0560724	intron-variant	RNF212	GRCh38.p7	4:1070217	GCTGTGCTGTGTCAG[C/T]GTGGGTGCCTGGCCT	285498
rs535140920	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1107745	ATGAGCCATCACGCC[C/T]GGCAGGACTTACACA	285498
rs535182650	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1073332	GGAAGCAAACCCAGT[A/G]ACACTATTTTTGTTT	285498
rs535215672	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1083709	TTAACCTGAAAATCA[C/G]GGAGCTGGAAGAAGC	285498
rs535220893	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1110443	CACATCCGCAGCCTA[C/G]CCACTCCACCCCGAA	285498
rs535320264	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1088521	GAACAAAATTGCAGC[A/G]CGACCATGCAGTAGA	285498
rs535360874	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1103827	ATTAGGAAAATGACG[A/G]GGGCGCCAGCTAATG	285498
rs535396966	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1100510	CTCCCCAGGTTCAAA[C/T]GATTCTCTAGCCTCA	285498
rs535400468	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1086149	GGGGGCCATGCAGAG[C/T]GAAGTCAAACCCAAG	285498
rs535639166	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1105341	CCACCACATCCCCAG[A/G]CACTGGCTTCAGTCT	285498
rs535681944	snp	A/T	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1065385	AGTTTGTTTCAGGTT[A/T]AACCATCTTCATAAA	285498
rs535689175	snp	A/G	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1085139	TAGCAGCCAGCAAAC[A/G]GGGGCTTGTGACTAT	285498
rs535732452	snp	G/T	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1113205	GCATCCCCCTCCCCC[G/T]GCCCCCTCCCCCTTC	285498
rs535819248	snp	C/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1057469	AGAGCAGGGGGAGGT[C/G]AACTGTGGTCTGTTC	285498
rs535820622	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1061573	GACTGGATATCGGCT[C/T]CCCACATGCACAGAT	285498
rs535862164	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1097656	AGTGCCTTCAGGATG[C/T]CCTGCCTCACCTCCC	285498
rs535884790	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1061724	AAAGAGCAGAAACCA[C/T]GAGCGGACACATCTG	285498
rs535886753	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1057169	GGCCAGCAGAAGATG[C/T]GGACCGATGCTGCAG	285498
rs535970422	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1097621	AAGCCCTCATGCAGA[C/T]GCTCCCAACTTCCTT	285498
rs535993030	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1101135	TGACCAGTATGAGCA[C/T]TGGCAGATGCTCTTT	285498
rs535993744	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1092984	AGCTCCAAACTACGC[C/T]AGGACCAGGGTCTGC	285498
rs536149782	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1075111	GGTGCAAACCTTTCT[C/T]GTAAATGGGCCATGG	285498
rs536167245	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1112068	AAAAAATCAGGGGTG[C/T]GTGGCTGCACATGCC	285498
rs536202018	snp	A/C	0.00199481	0.0315187	intron-variant	RNF212	GRCh38.p7	4:1065337	AATAAACATTTATTT[A/C]AAGGAAAACATCTGC	285498
rs536236620	snp	A/G	0.0023933	0.0345097	intron-variant	RNF212	GRCh38.p7	4:1092766	CTGCCCGGTGCTCAC[A/G]CGTGCTTTGCCCGCA	285498
rs536271919	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF212	GRCh38.p7	4:1071665	ATGCAGATGAAAAAT[C/G]AGCATAAGATGCTCC	285498
rs536277049	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1110188	GGATTGATGCCTGAT[A/C]TATAAATAGTGCTCA	285498
rs536290754	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1058888	ACGAGCTTCCTCCCC[C/T]GCCTCTCCCAAGCCT	285498
rs536321361	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1087961	TTCCTTTATAAATCA[C/T]CCAGTCTCAGGTAGT	285498
rs536338567	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1107993	ATTGATTTTAAACTT[A/C]CTTTATGAACAACAC	285498
rs536340617	snp	C/T	0.00953873	0.0683987	intron-variant	RNF212	GRCh38.p7	4:1065973	CCTTGACCTCCTGAG[C/T]TCAAGCAATCCTGCC	285498
rs536364456	snp	G/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1104743	GATGCTGGGGCAGCA[G/T]GTGGCCCCTTCCCTC	285498
rs536417569	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1060753	GTGTTCTGGAGGGGA[A/C]CGCGTACTGAAGAGT	285498
rs536420096	snp	A/C	0.000399281	0.0141238	downstream-variant-500B	RNF212	GRCh38.p7	4:1055960	GGGTGAGCTCAGGCC[A/C]GGAATTCATCTCTGG	285498
rs536426563	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1078505	CTCTGGTCTTGCTTC[C/T]CTCCAGCTTGAAGTT	285498
rs536455859	snp	C/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1081895	AGCACATGGCCACTG[C/G]GGGTGTTAAAGGTGT	285498
rs536478580	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1096555	AGTGCACCTGGCTCA[C/T]CACAGAACCAAGCAC	285498
rs536588614	snp	A/C	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1089276	TCCTGGATGTGAGAC[A/C]TTGGGTAAAAGGATA	285498
rs536591602	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1082367	ATGCTGAGATGCACA[C/T]GTAAGACTGGGGGAG	285498
rs536608175	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF212	GRCh38.p7	4:1072341	GACACATGTCACTAG[A/C]TATTTGTTCAAACCC	285498
rs536618243	snp	A/C	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1112032	TGGGCAACAAAGGGA[A/C]CCCATCTCTGTGAAA	285498
rs536648472	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1109763	AACAACCCACTTCAC[A/G]CTACCTCCTTCCTTT	285498
rs536665950	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1078002	TCACGGAAGCTGTGA[C/T]GGCTCTTCGTTCCCT	285498
rs536714688	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1099118	CAGTGAGGCCTGAGC[A/G]GGAGAACACAGGCAG	285498
rs536778935	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1104406	GGGCTCAGGTCACCC[C/T]GCCCCCAGCAGCTCT	285498
rs536820647	snp	C/T			intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1058271	GCTGTGAAGAAGGTG[C/T]TTGCGGGGGTTAGAA	285498
rs536822019	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1063104	TGGATTGGAAGATGC[A/G]GTGTTAGTATTAGAT	285498
rs536847641	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1099616	TCGCACAATCCCCAG[A/G]AAAATCACAAACGAA	285498
rs536883018	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1062513	AACCCTATAAAGGGC[A/G]CCTCCAGGAAACCCT	285498
rs536913810	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1085303	GAACAGATGCAATAC[A/G]GCAAAAGCACGGATG	285498
rs536957567	snp	C/T	0.000798403	0.0199641	synonymous-codon, nc-transcript-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1058350	CATGCTCCTCTGACT[C/T]GTTGTCAGGCCGGGA	285498
rs536975660	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1096657	TCCATGGTCTCGGGA[G/T]AGTGCACCTGGCTCA	285498
rs537020703	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1105756	CGTCCTTCCACCGCA[A/G]GTCAGGGTCAAAGAA	285498
rs537050829	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1085834	TCTTGGAGAGCCAGA[C/T]GACCAATGCACATGG	285498
rs537073428	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1094431	GGCTTGGAGTGGAGG[C/T]GCGTGCTGACTGGGA	285498
rs537088478	snp	C/T	0	0	intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1111729	AAATCAACAACTCCA[C/T]TCCCAGGTTACACAC	285498
rs537095480	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1101589	AATAGTTATGGTCAA[C/T]AGTTATAGAAAAATT	285498
rs537108469	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1107281	TGGTCTCGATCTCCT[G/T]ACCTCATGATCCGCC	285498
rs537126725	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1081362	TTGGGATGGGAAGGC[A/C]GGTGCAGAATCGGAA	285498
rs537137630	snp	C/T			intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1112398	CCACCGGCACCCAGC[C/T]GGCTGCTTTCACGGG	285498
rs537158896	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1106612	AGAAAGACACGGATG[G/T]TCTTAAATATACTTA	285498
rs537190197	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1080753	GTCCTCCCCACAGGC[A/G]CCCTCCCTGTCCAGG	285498
rs537206999	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1070161	AGGACTGCGCTGTGT[C/T]AGCGTGGACGCCTGG	285498
rs537243204	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1096112	ACACCCCCCACAGCT[C/T]CACGGTCTCGGGATA	285498
rs537245134	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1107650	AGAGATGGGGTTTCA[A/C]TGAGTTGGCCAGGAT	285498
rs537279287	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1080919	CTGTGCCAGAGTGAT[A/G]GCCAGGCAGGCATAG	285498
rs537279380	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1098912	GACCAAGAGCTCCAT[C/G]GACCAGAAATGGGAG	285498
rs537298370	snp	A/T			intron-variant	RNF212	GRCh38.p7	4:1077472	TCCTGGGCTCAAGTG[A/T]TCCACCTGCCTTGGC	285498
rs537362658	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1075332	TCATAAAGAAAAGAG[C/G]TTTAACTGGCTCATG	285498
rs537454725	snp	C/T	0.00398564	0.0444627	intron-variant	RNF212	GRCh38.p7	4:1064306	TTCAGTCGGTGTTCA[C/T]CTCAGTGAGTGTTCA	285498
rs537530437	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1078127	TGAGTTCATATCTAT[A/G]AAGGGCTCGGAACAG	285498
rs537535362	snp	A/G	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1076013	ATTTTGTATTTGTGA[A/G]TCATGATTTTACCTT	285498
rs537553380	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1110553	TGATAGCCAAAAGAT[A/G]TATCATGCAACCTTA	285498
rs537700322	snp	C/T	0.000185408	0.00962652	intron-variant, utr-variant-5-prime	RNF212	GRCh38.p7	4:1099818	CGAGTCCACAAGGTC[C/T]GACGGCGCAAGCGGA	285498
rs537700895	snp	A/G/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1058310	AGAAGGTGCTTGCGG[A/G/T]GGGGCACTACCTGAG	285498
rs537735870	snp	A/C	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1063892	AAAAAATGAAAAAAA[A/C]CAATATTAATAATAA	285498
rs537844944	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1094746	AAGCAACCTGCTGCC[A/C]TGAACCCAGAGAACC	285498
rs537897005	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1069790	AGGCCTTTATTCTTC[A/G]GAACTGTTGAGGACA	285498
rs538061393	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1072674	GGATAATAACAATAT[A/G]TATGAGTACATAAAA	285498
rs538135101	snp	C/G	0.00159617	0.0282053	intron-variant	RNF212	GRCh38.p7	4:1066568	ACTCCTGAGCTCAAG[C/G]GATCCTTTTGCCTTG	285498
rs538219518	snp	A/G	0.00279162	0.0372561	intron-variant	RNF212	GRCh38.p7	4:1063801	ATTGATTGAGCCCAG[A/G]AGGTCCAGGCTGCAG	285498
rs538226885	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1100353	TGCACAGCTTACTTC[C/T]GAGCTACTGGTGCAC	285498
rs538277380	snp	C/T	0.00159617	0.0282053	intron-variant	RNF212	GRCh38.p7	4:1067082	TAGTGTCTTTCTCCA[C/T]TGAATAGTGTGTTTT	285498
rs538366690	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1095161	ACCAAGCACGCCCCC[A/C]ACAGCTCCATGGTCT	285498
rs538442566	snp	C/G/T	3.29958e-05	0.00406165	missense, intron-variant, nc-transcript-variant	RNF212	GRCh38.p7	4:1090807	TAGAAGGCTAACAAT[C/G/T]TCTTCCTGTGTTTTT	285498
rs538444887	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1083797	CGAGGGTGGGGAGCT[A/G]CAGGTTGTGGCTGGG	285498
rs538508626	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1079571	GAGAGGTTACGTTTT[C/T]CACTACTGAGGAAAA	285498
rs538532285	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1081778	GTTCCCATAGCGTCC[A/T]GTGAGTCGCACGGCC	285498
rs538577693	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1084363	GGCTTTGCTGTCCAC[A/G]TAAGGTCTCCGTTGC	285498
rs538609768	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1070905	AATACTGTTCTTACA[A/G]TTTTTTCTGTGTGCT	285498
rs538628097	snp	A/G/T	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1106028	GCTTACTCCTGGAAA[A/G/T]TTGGGATGCATTTAA	285498
rs538672146	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1076371	TGGCTTTGCTTCTCC[A/G]AGTCCACCCAATGAG	285498
rs538714085	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1103886	AGGTCCCAGCCAATG[C/T]TGTAAAAAAAAGGAA	285498
rs538745677	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1064661	TATGATGATACAGTT[C/T]CCTACCTTAACCATT	285498
rs538763412	snp	A/G			utr-variant-3-prime, intron-variant	RNF212	GRCh38.p7	4:1072462	ACATGGACTGCTCTG[A/G]TGGAGGATGAGGATG	285498
rs538837838	snp	A/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1092966	CCTGCATTCGTCCAC[A/G]TGAGCTCCAAACTAC	285498
rs538874441	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1065276	GCTTCCAATTCCTCC[A/G]CGTCCTTAACAACAC	285498
rs538908858	snp	G/T	0.0123763	0.0776852	intron-variant, synonymous-codon, downstream-variant-500B	RNF212	GRCh38.p7	4:1093889	TGCCCGTGTTGTGCT[G/T]ACCCAGTGTTCTTGG	285498
rs538910802	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1088703	AGTTTTATGGGCCGG[A/G]CCAAGGCCCCCTGCC	285498
rs538972332	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1087882	CCCCCTTTGCCTTCT[A/G]CCATGATTGTAAGTT	285498
rs538973264	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1077463	GTCTTAAACTCCTGG[C/G]CTCAAGTGATCCACC	285498
rs539024531	snp	A/G	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1079523	CCAGCACACGAAGCA[A/G]CAGCACTGTGCAAAG	285498
rs539066682	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1085027	CTGACACAGCAGGGA[C/G]GTGGGCACCTGCACA	285498
rs539074990	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF212, LOC105374344	GRCh38.p7	4:1114445	GGGCCAAGTGACCCC[A/T]GCGCCCCGAAAGATG	285498
rs539084277	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1088713	GCCGGGCCAAGGCCC[C/T]CTGCCCAACTCTCGT	285498
rs539137968	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1074310	CCCCTTCCTGGGCTC[A/G]CTCCTCTGGCTCTCC	285498
rs539153786	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1108921	GCCCACACTGGGCTC[A/G]AACTCCTGGGCTCAA	285498
rs539272869	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1069977	CCTAGCCTGAATTAC[A/G]GGTGGTTTTGTAGGA	285498
rs539316620	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1091540	GTACTGAAAGTCGGC[A/G]TCCTCTAGCTCCATC	285498
rs539320631	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1060296	CCCTGCCGATCAGCC[C/T]GCTGTGTGTCCCACA	285498
rs539321516	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1096027	GCACCTGGCTCATCA[C/T]GGAACCAAGCACACC	285498
rs539345102	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1099023	ACACCCCAGGATGTC[C/T]AGAAGATGAGCCTAG	285498
rs539376629	snp	A/C	0.00398564	0.0444627	intron-variant	RNF212	GRCh38.p7	4:1095600	GGTCTCAGCATAGCG[A/C]ACCTGGCTCATCACA	285498
rs539386264	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1101532	GTTCCTACTAATTCT[C/T]CAGAATGAATAAGTT	285498
rs539473937	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1105731	GTGCACATGCTGGCA[C/T]AATATAAAGCGTCCT	285498
rs539584082	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1061747	CACATCTGCGGCTGC[C/T]GTGGACACAGATTCT	285498
rs539610974	snp	A/C	0.0023933	0.0345097	intron-variant	RNF212	GRCh38.p7	4:1101124	TTGAGTTGGTGTGAC[A/C]AGTATGAGCATTGGC	285498
rs539623536	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1113268	CGTGCCCCCATGGCC[C/G]TCCCACCCAAGTCCC	285498
rs539669594	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1080683	TGCTGGCCCACGAGA[A/C]CCCTCTCTGCCTGAG	285498
rs539859124	snp	C/T	0.000399281	0.0141238	synonymous-codon, intron-variant, nc-transcript-variant	RNF212	GRCh38.p7	4:1081586	AACTGAACTTTTTAT[C/T]GTGCTGAAAGCTGTT	285498
rs539963349	snp	G/T			intron-variant	RNF212	GRCh38.p7	4:1082924	CTAAAATGCACTGTT[G/T]CGTGGGAGCAAGAGG	285498
rs539972433	snp	A/C	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1085250	GGCCTGTTATTGATT[A/C]CAAATTCCAGAAATG	285498
rs539986150	in-del	-/AC/GC	0.350109	0.229081	intron-variant, frameshift-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1093540	GGGCAGAGCCTGTGA[-/AC/GC]CCTCCACGGCCCATG	285498
rs539991292	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1075838	ACCATGCCCAGCTAA[C/T]TTTTTGTAGAGATGG	285498
rs540004289	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1064869	TCTACGATCTTGACT[A/G]CTTCACACACATGGA	285498
rs540004884	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1104499	TTTTATGGGCCAGGC[C/T]TGGAAGTGGTCTTCA	285498
rs540033010	in-del	-/GA	0.491525	0.0645418	intron-variant	RNF212	GRCh38.p7	4:1087164	AGAGGATGGGTGGGG[-/GA]GAGAGGATGGCATTG	285498
rs540050923	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1075204	TGTTCACATCTGCAT[A/T]TGGCTGCCTACACGC	285498
rs540095687	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1108602	TCTTTTCCCCTCTTT[C/T]GCAAATATGTACAAA	285498
rs540124119	snp	C/G	0.00438332	0.0466095	intron-variant	RNF212	GRCh38.p7	4:1069545	CTCCTGGAGGAATCA[C/G]GCGACCAAGGTGAAC	285498
rs540330694	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	RNF212	GRCh38.p7	4:1055988	TGGACCTGACGGAGA[C/T]TCACCCGCTGAAGCC	285498
rs540343480	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1082667	TGTCCCGGCCCGACA[C/T]ACAAGTTCACTTTCT	285498
rs540367816	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1076702	TCCAGGGTGACAAGG[C/T]GTTTCGGGAGGTGAA	285498
rs540381910	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF212	GRCh38.p7	4:1071922	ACACTCCTTAGTATT[C/T]ACCCAAAGGAGCTGA	285498
rs540401425	snp	C/G/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1109256	CAGGTGATCAGCCCA[C/G/T]ATCGGTCTCTCAAAG	285498
rs540539692	snp	A/G/T	0.00173215	0.0293795	intron-variant	RNF212	GRCh38.p7	4:1085879	ACTGCGCACTCACGG[A/G/T]GGGTGGGGCGCCTTA	285498
rs540575553	snp	A/G			intron-variant, utr-variant-5-prime	RNF212	GRCh38.p7	4:1099882	TCCTCACGCAGCTGT[A/G]AAGGCGTGCTGTTGG	285498
rs540598825	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1057415	GTGTGTGCTTAAATA[C/T]GCAGCAGACGGAGTG	285498
rs540621160	snp	C/T	0.000607718	0.017421	intron-variant, missense, downstream-variant-500B	RNF212	GRCh38.p7	4:1093660	CTGGCCTCTGCAGCA[C/T]TTGGCAAAACCACCC	285498
rs540653854	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1061935	ACCACACTCAGGGAA[A/G]AGGGCAGATGGCAGA	285498
rs540695405	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1089294	GGGTAAAAGGATAAA[C/T]TTAAGATTTAATGGC	285498
rs540743704	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1091652	CGGTGCAAACACAGG[A/G]CAGGCTTCTTCCCTC	285498
rs540807966	snp	A/G			intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1111971	ATCCCACATTTCGGG[A/G]GGCCAAGGCCGGTGA	285498
rs540878672	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1085488	AACATGCCACATATA[C/T]GTACCTTTCGCAAAC	285498
rs540905497	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1075318	AGAGACTGTGTAATT[C/T]ATAAAGAAAAGAGGT	285498
rs540911745	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1080832	GAATTTGTGCCTTCC[A/G]TCTGAAGAGCTAGGA	285498
rs540973415	snp	A/G	0.00199481	0.0315187	intron-variant	RNF212	GRCh38.p7	4:1080417	TCCAGTTCTCCACCC[A/G]CTCCCAGTGTCTCAG	285498
rs541026733	snp	A/G	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1095774	CATGGTCTCAGCATA[A/G]CGCACCTGGCTCATC	285498
rs541085802	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1096946	CTATAGATGACTCAA[A/G]TGGCCAGCACATTGT	285498
rs541101979	in-del	-/A			intron-variant	RNF212	GRCh38.p7	4:1088678	ATCATAGGCCCAGAG[-/A]AAAAAAAGTAGTTTT	285498
rs541119701	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1095335	AGAACCAAGCACACC[C/T]CCCACAGCTCCATGG	285498
rs541122571	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1057323	TCAAGGGCTCTGGGG[C/G]GCTGACATGGGAGGG	285498
rs541136688	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1073720	GCGGCTTACGAGATT[C/T]GGACTCCCACTGTCT	285498
rs541158702	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1063564	AAACTAGCCAGGTGT[A/G]GTGGTGCGCACCTGT	285498
rs541165584	snp	A/G	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1096307	CGGTCTCGGGATAGC[A/G]CACCTGGCTCATCAC	285498
rs541225353	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1097333	TCGTAGGTCGGGAGC[A/G]GTGGCTCAAGCTTGT	285498
rs541337965	snp	G/T	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1087524	GTGACAGGATGAGGT[G/T]GGGGGGTGACAGGAC	285498
rs541408307	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1104251	CCTCCAAAATTTATG[C/T]GGACATGCGAAGATG	285498
rs541429623	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1069125	CTGAGGCACAAGAAT[C/T]GCTTGAACCTGGGAG	285498
rs541443305	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1078237	ACACAGGCATTCACC[A/G]CCGCCAGAACACACT	285498
rs541456305	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1106927	GTTAAAAATGTTCAC[C/T]GGAAGGTTGTTTGAA	285498
rs541479189	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF212	GRCh38.p7	4:1072111	CTAGCAAACCATGAG[A/G]AGAGATGGGGGAACC	285498
rs541505520	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1109625	GCTTTTCCTGGGTAT[C/T]TTCTGCCCCATTCCC	285498
rs541611387	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1092280	CTGATCCTGATTTGG[A/C]AGGGCAGGTGTTGCT	285498
rs541624975	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	RNF212	GRCh38.p7	4:1099852	GGGTACCCCTGTGCG[C/G]GATCCACGGGGCTCT	285498
rs541642032	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1064091	CTGGAAATGGTTAAT[A/G]TGTTGTGAATGATGG	285498
rs541793572	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1089395	ATGGGAACATTTACC[C/T]AATGCCTGTACTCCC	285498
rs541864921	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1090370	AGCGGCCCCAGGTTC[A/C]CTTGTCTTTAAAGCT	285498
rs541922792	snp	C/G			upstream-variant-2KB, intron-variant	RNF212, LOC105374344	GRCh38.p7	4:1113838	GCGACAGCAGTGGGG[C/G]AGGGGGAGGGGGAGC	285498
rs541965107	snp	A/C	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1110797	GCCCAGAGCCTCCAC[A/C]CCTTTTCACCACTTT	285498
rs541983841	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1098834	CCATGTGAGTGCGCA[C/G]GGAGCGGGAACTGTC	285498
rs542012265	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1074528	TGTCCTCATGGTCTC[C/T]CTACCAGCACAGGAG	285498
rs542110652	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1061568	GAACTGACTGGATAT[C/T]GGCTCCCCACATGCA	285498
rs542178130	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1105904	GCCAGGCACTGAGGC[A/G]GACGAAGACCCTGGC	285498
rs542263521	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1059474	GAGGCAGGAGGCCAC[A/G]GTGAGCACACTTCTG	285498
rs542285539	in-del	-/TTAA	0.00159617	0.0282053	utr-variant-3-prime, nc-transcript-variant	RNF212	GRCh38.p7	4:1056287	ATTCCACTACATTAC[-/TTAA]TTATTTCAACAAGAG	285498
rs542325960	snp	C/G	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1079285	AACACAGGGTCAACA[C/G]AAGACCAACATGGGA	285498
rs542394030	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1105543	GTCACTTTTACATGG[C/T]AGTGTCTGTCACAAT	285498
rs542425135	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1073919	GCCTAAAACAGTGAA[C/T]GGATAAAGGGCTCTA	285498
rs542453530	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1111340	CTCCCCAAATGTGTT[C/T]CTGGCTGTCTTGAGT	285498
rs542499298	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1101216	AGTGCAGTAGCCGTG[A/G]TGGCATCTCTACACA	285498
rs542540986	in-del	-/A	0.0456336	0.143994	intron-variant	RNF212	GRCh38.p7	4:1095213	CACAGAACCAAGCAC[-/A]ACTCCCCACAGCTCC	285498
rs542560351	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1100720	GGCCGCGTTTTCCAT[A/G]TTGAAGTTCCAACTT	285498
rs542571440	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1059465	CAGTTCCTAGAGGCA[A/G]GAGGCCACGGTGAGC	285498
rs542683726	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1091938	GGACAGAAGGACTCC[A/G]CAGGTTGCCCTGACC	285498
rs542687279	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1076099	ATTTAAGGTTAACAG[C/T]CTTAACTTAGAAATT	285498
rs542712691	snp	C/T	0.000446742	0.0149389	intron-variant	RNF212	GRCh38.p7	4:1081552	TTGTTCTCTTTCTGG[C/T]ATGATTTTACTTACT	285498
rs542715413	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1106531	TTAAAAAAATAAAGA[C/T]ATATTAGAGATTATT	285498
rs542726504	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1088161	GGAACTTCCTAGAGA[A/G]TTGTTGAATGGTTTT	285498
rs542773933	snp	G/T	0.0256215	0.110247	intron-variant	RNF212	GRCh38.p7	4:1087281	AGGATGGGGTGGGGG[G/T]GAGAGGATGGGTGGG	285498
rs542846444	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	RNF212	GRCh38.p7	4:1056329	CAGTCGCACTGGCTG[C/T]CTAACGTACACATGC	285498
rs542867710	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1099204	GGAATTTTCAAAGTG[C/T]TAAGATGCATTCACT	285498
rs542893236	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1077844	AGGGAGGAGGTGCAC[C/T]CATAAGGAAGCGTGT	285498
rs542895031	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1082970	ACAATGACAACAAAA[A/G]TGGGTGGCACGAACG	285498
rs542895749	in-del	-/TGA			intron-variant	RNF212	GRCh38.p7	4:1073972	AACAAAATTTGCAGC[-/TGA]TGTTAGAGAATGTGA	285498
rs542958546	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1082627	CTCAACATCCTCACC[C/T]AGAGTCACTTATCCT	285498
rs542976636	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1061484	CCTGGAACCCTGGCC[A/G]ACAGAAGCAGCACAG	285498
rs543038712	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1068284	TCATCGACAGGGTCC[A/G]GAAGAAAGCCCTCAC	285498
rs543104747	snp	C/G	0.0126979	0.078662	intron-variant	RNF212	GRCh38.p7	4:1095650	CAGCTCCATGGTCTC[C/G]GGATAGCGCACCTGG	285498
rs543138121	snp	A/G	0.00279162	0.0372561	upstream-variant-2KB, intron-variant	RNF212, LOC105374344	GRCh38.p7	4:1114194	TCCAGGTGGCCGCTG[A/G]CGCAGAGACCTCAGC	285498
rs543203897	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1090981	GCCCCCACAGACGCC[C/G]ATGGCCAGTGCTTGC	285498
rs543258129	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1064850	CACCATCCTACTTTC[C/T]GTCTCTACGATCTTG	285498
rs543344006	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1084601	TGTGTGTGGTGGTGC[A/G]TGCCTGTGGTCCCAG	285498
rs543384079	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1100661	TGATCTGCCCGCCTC[A/G]GCTTTGCAAAGTGCT	285498
rs543414385	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1095145	CCTGGCTCATCACAG[A/G]ACCAAGCACGCCCCC	285498
rs543472871	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1101835	TAAACTACTTTCCTT[C/G]ACCTAAATGTTGGTT	285498
rs543482786	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1105438	AATGGAGCATTATAA[G/T]GACAAACAAATCAAT	285498
rs543520492	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1095390	TCACAGAACCAAGCA[C/T]AACTCCCACAGCTCC	285498
rs543521429	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1092187	ACCTACCAGCAGACG[C/T]GCCTCATCCCGGCTG	285498
rs543531926	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1106853	CTTTTGCCCTTGCTT[C/T]TTCATTACTTCAGGA	285498
rs543598651	snp	A/G	0.00358779	0.0422022	intron-variant	RNF212	GRCh38.p7	4:1075293	CCATTCTTGCACTGC[A/G]ATAAATACCAGAGAC	285498
rs543669307	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1079874	CTCTTTAGGGCCACC[C/T]GCCGTCTGTACTGGG	285498
rs543699529	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1058610	GAAGCCCTGGGTCTT[C/T]CACATGAGGGCGTAA	285498
rs543740663	snp	G/T			intron-variant	RNF212	GRCh38.p7	4:1078699	ACACCAACAGAGACT[G/T]ACAGGGACCAGCACG	285498
rs543752367	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1076410	GCACTGTGGCCCTCC[C/T]TCTGACGAGCCTTTG	285498
rs543769487	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1108760	TGATCTGCAAGTGGC[A/G]TGATCACAGCTCACT	285498
rs543774187	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1057146	CAGCACGCACACCCC[C/T]GCCCGGCGGCCAGCA	285498
rs543795828	snp	C/T	1.648e-05	0.0028705	intron-variant	RNF212	GRCh38.p7	4:1096866	AGAAATGACTCTACA[C/T]TTATTGTGTCTAATA	285498
rs543806826	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1074769	AAGAAGACAGAATCT[C/T]GTGAAATCAGGAGCT	285498
rs543846359	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1111922	AAAGTAGATGAACTA[C/T]AGTTACATACAAATA	285498
rs543890862	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF212, TMED11P, LOC105374344	GRCh38.p7	4:1114811	AGCAAATTAGAATTA[C/T]GTATGTAGCCCACTT	285498
rs543953385	snp	A/G	0.0103295	0.0711199	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1058252	TGCTTGCGGGGGTTA[A/G]AACGCTGTGAAGAAG	285498
rs543980819	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1104533	CTCCTGCTTGCATTT[C/T]AGCATGGGAAGGTAG	285498
rs543991466	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1063523	TGAGACCAGCCTGGC[C/T]AACATGGTGAAACCC	285498
rs543992093	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1096508	TCATCACGGAACCAA[C/G]CACACCCCCCACAGC	285498
rs544038528	snp	C/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1060127	AAGAAAAAAGAAATT[C/G]TTTCCTATTTACTCA	285498
rs544050165	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1062740	AGATAAATAAAAGGC[A/G]TCGTGGTTGGAAAGG	285498
rs544088229	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1106709	CACCAGCCTCCAGCC[C/T]GACCGTGTACAGGGC	285498
rs544235828	in-del	-/ACAAT	0.00159617	0.0282053	intron-variant	RNF212	GRCh38.p7	4:1068547	TTTGTTATAACTCCA[-/ACAAT]ACAGTGTTATCATTG	285498
rs544252955	snp	C/T			intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1112041	AAGGGACCCCATCTC[C/T]GTGAAAAATTAAAAA	285498
rs544342509	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1077790	CTTCCAGCAGGGCCT[A/G]AGGGGGCAGGTGGGG	285498
rs544350678	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1078379	CCTCTCTCCCGTTTC[C/T]GAGCTGCCTGGTGTG	285498
rs544371090	snp	A/T	0.000399281	0.0141238	downstream-variant-500B, intron-variant	RNF212	GRCh38.p7	4:1071116	TTTAAAAAACTAATT[A/T]GTTTTTTTAAATACT	285498
rs544383298	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1066028	ACAGGTGCGATTTTT[A/T]AAATATATAGTAGCC	285498
rs544444207	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1065616	GGGACCACAGGTTTA[C/T]GCCACCAGCCTGGAT	285498
rs544450201	snp	C/T	0.000798403	0.0199641	intron-variant, missense	RNF212	GRCh38.p7	4:1094211	AGGTGGGGTGGCCAA[C/T]GGTGGGAGCTGCACT	285498
rs544485801	snp	G/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1066829	TGTTTAATTTTTTTT[G/T]TTGTTGCCTGTGCTT	285498
rs544513148	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1099234	TTTCAACAAAGAATT[A/C]TGAAGTCTGTGAAAA	285498
rs544581207	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1102354	AGTTGGCCTTGTAGA[A/C]CCTGCATACAGGAAA	285498
rs544627678	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	RNF212	GRCh38.p7	4:1056051	CCAGAATGCGTAGTA[A/G]TCACCTAACGCAGGA	285498
rs544629859	snp	C/T			intron-variant, missense	RNF212	GRCh38.p7	4:1094355	AGGCCAGAAGTGCCA[C/T]TCAGCATGTGGGGGT	285498
rs544706848	snp	A/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1058219	CTGACAATTTCCTTT[A/T]AAACGCTGTGAAGAA	285498
rs544746837	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1089777	TGATGGTTTAAGAGT[A/G]TTTGGCAGTTCCCCC	285498
rs544746928	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1083016	CGGGCAAGACGGGGT[C/T]GGGGGCGCAGCGGTC	285498
rs544776862	snp	G/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1070881	ATGTTGGAGTTTTGT[G/T]TTTTTTTTAATACTG	285498
rs544799092	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1078768	AACACAGAACCAACA[C/T]AGGACCAATACAGGG	285498
rs544806228	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1110598	GACTTATTTTAACAC[A/G]GAAGGAGGTCTATGT	285498
rs544923090	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1111289	TCTCCACACTCCAAT[A/C]TCTAGGATTATAGGA	285498
rs544923102	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1087581	GGTGTGACAGGAGCA[A/G]GGAGTGGGTAATAGG	285498
rs544934556	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1073463	ATTTTGGTGAATATG[C/T]AGCCTCCCATGCACC	285498
rs544943868	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1105139	CAAAAGCAACTGGCG[C/T]GTCCATGACTGTGGG	285498
rs544958234	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1110913	GTTGACCTCAGGCTT[C/T]AAGAGCTAGGCAAAC	285498
rs545009041	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1091768	AGGGGCCCTCCTCCA[G/T]GACAGCAGGGATGAC	285498
rs545025124	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1070323	ACTGTACTGTGTCAG[C/T]GTGGACGCCTGGCCT	285498
rs545052534	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1080535	CACCCTTCATTGACC[A/G]TACAGATGTACCACA	285498
rs545089923	snp	C/T	5.00188e-05	0.00500069	intron-variant	RNF212	GRCh38.p7	4:1085874	CCTCGACTGCGCACT[C/T]ACGGGGGGTGGGGCG	285498
rs545117149	snp	A/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1085558	GGTGGAGTCCCGCAG[A/T]CCCTGGCTGCAGGGC	285498
rs545189502	snp	C/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1093164	GACGCTGTCCCAGGG[C/T]AGGTCCTGAGGCCTG	285498
rs545190274	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1097387	AGGCGGGCGGATCAC[A/G]AGGTCAGGAGATCGA	285498
rs545320797	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1088095	GGTAATGGGCAGAAG[C/T]TGGAACAATTTGGAG	285498
rs545323122	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1107328	AGTGCTGGGATTACA[G/T]GTGTGAGCCACTGCG	285498
rs545325253	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF212, LOC105374344	GRCh38.p7	4:1114036	TGGGTGTGGGAGTTG[C/G]GGTGGGAGCGGGAGT	285498
rs545330602	in-del	-/T	0.0023933	0.0345097	intron-variant	RNF212	GRCh38.p7	4:1108685	TTATTACAATTAGGC[-/T]TTTTTAAAATTAAAA	285498
rs545342290	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1082029	GCAGGGGCGGGAGGA[C/T]TGGTTGAGCCCAGGA	285498
rs545418456	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1089749	TCTCGTGATAGTAAG[C/T]TCTCATGAAATCTGA	285498
rs545452352	snp	C/T	0.00398564	0.0444627	intron-variant	RNF212	GRCh38.p7	4:1082536	CAAGCCAGCTAGGAA[C/T]AGGCAGTTGCACAAC	285498
rs545492499	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1062864	ACTCAGTAGATTGCA[A/G]GATACAAGATCCATC	285498
rs545534904	snp	A/C	0.00279162	0.0372561	intron-variant	RNF212	GRCh38.p7	4:1100634	GGCTGGTCTCAAACG[A/C]CTGACCTCAGGTGAT	285498
rs545582503	snp	C/T	0.127254	0.217792	intron-variant	RNF212	GRCh38.p7	4:1095244	ATGGTCTCGGGATAG[C/T]GCACCTGGCTCATCA	285498
rs545618133	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1059346	AGCAAGAAGGAAAGC[C/T]GTCTTACTAGGCTGT	285498
rs545711591	in-del	-/ACATAGCACAT			intron-variant	RNF212	GRCh38.p7	4:1067989	CTAATCAATGGAGAG[-/ACATAGCACAT]CTAAGCACTGAGACA	285498
rs545736754	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1066681	GTTTTAGTTCTTTAT[A/G]TATTCTGGATTGTAA	285498
rs545756368	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1111464	CCCCACCCTGCTGTG[A/C]CCCACCCTGCTGGGT	285498
rs545873575	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1060979	ATCTCTACGAAGCCA[A/C]GTGCGAAACTGGACA	285498
rs545878429	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1084533	TCAGGAGTCCAAGAC[C/T]AGCCTGGGTAACATA	285498
rs545989031	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1057231	CAGGCCAGCGGGGAC[A/G]GGAGGTGGGGGCGTG	285498
rs546020642	snp	C/T			upstream-variant-2KB, intron-variant	RNF212, TMED11P, LOC105374344	GRCh38.p7	4:1115526	AATATCTTACACCAA[C/T]GTATCCGTGCAGTCT	285498
rs546040923	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1084039	CCGCAACCTCTGCCT[C/T]CCAAGTTCAAGAGAT	285498
rs546130363	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1096475	ACAGCTCCACGGTCT[C/T]GGGATAGCGCACCTG	285498
rs546147997	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1075361	TGCTTCTGAGGGCCG[C/T]ACAGGAAGCATGGCA	285498
rs546163102	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1098429	GTCCTGGAATCCACT[C/T]CAGAATCCACTCCCA	285498
rs546179739	snp	A/G	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1079341	ACATGGGACCTGTAC[A/G]GGAACAACACAGGAA	285498
rs546306894	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1074646	GGAAGGACGGACCCC[C/T]CTGCTTGGCATGGCC	285498
rs546341084	snp	A/G	0.00159617	0.0282053	intron-variant	RNF212	GRCh38.p7	4:1059109	TTAGGCTTCCCCAGC[A/G]CAGTGACTGTGACTG	285498
rs546350912	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1099550	AGAGCTGAGGCCCTC[A/G]CATCATCAAGAAAAC	285498
rs546359175	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1101376	GTTGAACTTTTCTTC[C/T]CTTTCTAAACTTTTC	285498
rs546370131	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1073994	AGAGAATGTGAAATT[C/G]TGAGTAAATCATTCT	285498
rs546404444	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1058786	TCGGCCCGTGGGCTC[C/T]GCGAGGGGAGCCTGC	285498
rs546467357	snp	A/G	0.00358779	0.0422022	intron-variant	RNF212	GRCh38.p7	4:1057831	GCACCTTGGGAGGCC[A/G]AGGCAGGCAGATCAC	285498
rs546467923	snp	A/G	0.00159617	0.0282053	intron-variant	RNF212	GRCh38.p7	4:1102847	ACAGAGCGAGACTCC[A/G]TCTCAAAAAAAAGGC	285498
rs546532031	snp	A/G	0.00159617	0.0282053	intron-variant	RNF212	GRCh38.p7	4:1095886	CAGCTCCATGGTCTC[A/G]GCATAGCGCACCTGG	285498
rs546619837	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1076225	GGCCTTAGGCTCTGC[C/T]TCTCCTCCTCCCCAG	285498
rs546663978	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1077389	CAATTTAGCCTGCCA[G/T]TCTTTTCTTTCTTTT	285498
rs546667025	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1081770	ATTCAGCAGTTCCCA[C/T]AGCGTCCTGTGAGTC	285498
rs546738681	snp	A/T			intron-variant	RNF212	GRCh38.p7	4:1088364	AGATGATTTAGGGCA[A/T]CTGGCAGAAGAAATT	285498
rs546757013	snp	A/G/T	0.00279162	0.0372561	intron-variant	RNF212	GRCh38.p7	4:1097474	GCCGGGCGTGGTGAC[A/G/T]GGCACCTGTAGTCCC	285498
rs546790444	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1077901	GCCGGTGGGTGTGGG[C/T]GTGGCCATGAGGATG	285498
rs546793175	snp	A/G	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1097476	CGGGCGTGGTGACGG[A/G]CACCTGTAGTCCCAG	285498
rs546814128	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1102958	CATCCTGGCTAACAG[A/G]GTGAAACCCCCGTCT	285498
rs546841183	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1103855	ATGCCACCGTTTCTC[C/G]TCAGCACTGTACTGG	285498
rs546854464	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1097048	CTCTGAGGGCTGTGC[A/C]GGACAGTGGTGAGGG	285498
rs546882548	snp	A/G	0.00318978	0.0398085	intron-variant	RNF212	GRCh38.p7	4:1061427	AGTCAGAAAAATAAC[A/G]GGGAAATGCTGAGAA	285498
rs546904358	snp	C/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1108913	ACTATGTTGCCCACA[C/G]TGGGCTCGAACTCCT	285498
rs547074201	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1090600	TAACTACAGACAAGG[G/T]TTGGGCAAATAGGCT	285498
rs547096936	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1082145	GGAAAAGGAAGGGGA[A/G]AGGGAAAGGAAAGAA	285498
rs547105570	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	RNF212, TMED11P, LOC105374344	GRCh38.p7	4:1115128	AAAAGCATTCTCTCA[A/G]TGTTATAATGATATA	285498
rs547191965	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1074223	ACTGGTAAGGGAGGC[G/T]GCTCTGCTCTGAGCC	285498
rs547200128	snp	A/G	0.00159617	0.0282053	intron-variant	RNF212	GRCh38.p7	4:1079927	GCCGCTGGCCGGCCC[A/G]CCCTGGTTGGGCTCT	285498
rs547211360	snp	C/T	0.00159617	0.0282053	intron-variant	RNF212	GRCh38.p7	4:1084163	TCCATGCTGGTCAGG[C/T]TGGTCTCAAACTCCC	285498
rs547244061	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1111967	GCTAATCCCACATTT[C/T]GGGAGGCCAAGGCCG	285498
rs547277786	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1104292	AACTGGTGTATCAGA[C/T]AACCCCCAAATCTCA	285498
rs547295027	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1100973	GGCTGAAATCACCTG[C/T]TAGCTCTTCCATATT	285498
rs547326162	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1074922	CTGGATCCTTCCATC[C/T]GCTAGGATGTCTTCA	285498
rs547364826	snp	C/T	0.0221141	0.102801	intron-variant	RNF212	GRCh38.p7	4:1096002	CACAGCTCCATGGTC[C/T]CGGGATAGCGCACCT	285498
rs547364922	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1102041	TAAAAATATAGTATC[A/G]TCAAATACATATACT	285498
rs547488447	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1062328	CACAGTTCCTTCAAC[A/C]TACAGAAATCAACAC	285498
rs547506477	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1077121	TAGTCCCAGCTACTC[C/G]GGAGGCTGAGGCAGG	285498
rs547535697	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1105709	ACACGGATGCACCCA[C/T]GTGCAAGTGCACATG	285498
rs547601302	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1111604	AACCTATCACTTCTC[C/T]CCATCACCTCTCATG	285498
rs547644592	snp	C/T			intron-variant, missense, downstream-variant-500B	RNF212	GRCh38.p7	4:1093951	TCGAGCCTCTGGGCA[C/T]CTCCTTGGAGGATGT	285498
rs547665783	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1097238	TAAGTCACCACTATG[C/T]AGTCACAAGTACATG	285498
rs547676862	snp	G/T	0.162253	0.234095	intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1113206	CATCCCCCTCCCCCT[G/T]CCCCCTCCCCCTTCT	285498
rs547710150	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1067853	AGCCTGGGCGACACA[G/T]CGAGACTCTGTCTCA	285498
rs547764390	snp	G/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1057905	CCCCTCTACTAAAAA[G/T]ACAAAATTAGCCGAG	285498
rs547769184	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1098183	TTCAGGACAGTGAGC[A/G]CATAGAGTCAAGACA	285498
rs547828501	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1103803	AAATACTGGAAGCTT[A/G]ACCCTGAAATTAGGA	285498
rs547905894	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1098831	GGCCCATGTGAGTGC[A/G]CAGGGAGCGGGAACT	285498
rs547938028	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1088549	AGAAAAGAAAAACCC[A/T]TTTTCTGAGGGGAAA	285498
rs547983894	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1058889	CGAGCTTCCTCCCCC[A/G]CCTCTCCCAAGCCTT	285498
rs548297935	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1060207	GACCCAAGAGGCCAA[A/C]AATTCACCCAGGGTC	285498
rs548314796	snp	G/T			utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1072641	ACTCCCTAAGCATGA[G/T]AACCTATAAAATAAA	285498
rs548321409	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1109767	ACCCACTTCACGCTA[C/T]CTCCTTCCTTTCTGC	285498
rs548325451	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	RNF212	GRCh38.p7	4:1056437	CAAGGTGAGCAGGTC[C/T]CGCAGGAGGCATGGA	285498
rs548356874	in-del	-/C	0.445328	0.156035	intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1113073	TCTCACCCCCCCATG[-/C]CCCCCCCCGCTCCAT	285498
rs548372190	snp	C/T	0.0023933	0.0345097	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1073509	ACCCCCTTGGGTAGG[C/T]TCTGACAGCTTTGAT	285498
rs548403166	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1072803	AAGGAATAAAGCAGA[A/T]AATTTGTAGAAAAAA	285498
rs548432131	snp	C/G	0.000399281	0.0141238	downstream-variant-500B	RNF212	GRCh38.p7	4:1055783	ACTAAAAGATTAGAA[C/G]TAACCCCATAAGCCT	285498
rs548469197	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1078011	CTGTGACGGCTCTTC[C/G]TTCCCTACTGGATCC	285498
rs548476700	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1083106	GCGATACCAGGTATG[C/T]AGAGAGTGGGATTGG	285498
rs548533038	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1110203	CTATAAATAGTGCTC[A/G]CTAGTCAATTAGAAA	285498
rs548538371	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1082735	GCACTGGGCGTGTTT[A/G]GCTTACTCCGAATTG	285498
rs548671809	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1104829	TCCTCGCCATGACCT[A/G]ACATCTAATGGCGGC	285498
rs548674218	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1112988	TCCCCCTCTCCCCAC[A/G]GGCCCCTCATCACGC	285498
rs548722321	snp	C/G	0.000399281	0.0141238	synonymous-codon, nc-transcript-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1058356	CCTCTGACTCGTTGT[C/G]AGGCCGGGATGCTCG	285498
rs548785643	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1069323	ATGACAATTAATACA[A/T]ATAGAAGGAACTGTG	285498
rs548786654	snp	C/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1094576	GGGGCTCAGCTGCCA[C/G]GATGGGGGCCCATGG	285498
rs548824101	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1090131	GGTGACAGGACAGGG[A/G]TGGGGTACCAAGATA	285498
rs548847234	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1075507	AACCAGCCAGATCTC[A/G]TGAGAACTCACCCAC	285498
rs548847983	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1099644	GAATGTTTTCTTTTC[A/G]TATTTAATTTTTAAA	285498
rs548856027	snp	C/T	0.00279162	0.0372561	intron-variant	RNF212	GRCh38.p7	4:1058756	CAGCTGAGTTTCAGC[C/T]TCACTGAGGGGCCCT	285498
rs548923165	snp	C/G	0.00159617	0.0282053	intron-variant	RNF212	GRCh38.p7	4:1095121	GCTCCATGGTCTCAG[C/G]ATAGCGCACCTGGCT	285498
rs548967811	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1092564	GACACTGGGTGTGGC[C/T]TCAGAAGAGGGTAGA	285498
rs548997727	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1112063	AATTAAAAAAATCAG[A/G]GGTGCGTGGCTGCAC	285498
rs549007045	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1080589	ACCCCGTGGAGCTTG[C/T]GCCTGCCTGCTCTAA	285498
rs549008400	snp	C/T			downstream-variant-500B, intron-variant	RNF212	GRCh38.p7	4:1071352	TATTAAAAAAACTCA[C/T]CTTACAACATACCTC	285498
rs549032937	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1096997	TGCCAGGGACAGCCT[C/T]GATCAACAGGACAGC	285498
rs549038128	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1081740	TACTGGGTTTGCAAA[C/T]GGCATTTCACATGAA	285498
rs549178219	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1069996	GGTTTTGTAGGATTG[C/T]GCTGTGTCAGCGTGG	285498
rs549180886	snp	A/C	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1102598	ACACAAAAAAACAAA[A/C]AAAAAACACTTTGGG	285498
rs549214430	in-del	-/C			intron-variant	RNF212	GRCh38.p7	4:1089237	CCAAGGCCTTGGGAG[-/C]CCCCCTACCCTTAAA	285498
rs549259424	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1088217	ATGGTGAAGTTCAGG[C/T]TGAGGAGGTCTCAGA	285498
rs549273511	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1103120	TGGATAACAAGCATA[C/T]TGATGACAAGAAATT	285498
rs549282119	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1108230	AGATATCTTTGTTAA[C/T]GGAGCAAAGTGACTG	285498
rs549308162	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1077301	TCTTTGCCCCTCACT[C/T]AGGAACTTTGATTCA	285498
rs549354071	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1092859	ACTCACGCGGACTCT[C/T]GCCAAGAGGCCAGGA	285498
rs549497785	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1083260	TGACTACATAAAAGA[C/T]GAAGATGCAACAATG	285498
rs549523931	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF212, TMED11P, LOC105374344	GRCh38.p7	4:1115043	GTGCAGCAGAGCGAG[A/T]CTCAGTCTCAAAAAT	285498
rs549630225	snp	A/T	0.000399281	0.0141238	downstream-variant-500B, intron-variant	RNF212	GRCh38.p7	4:1071262	AAAATAAATTATTTT[A/T]AAAAAACTAACTTGG	285498
rs549660656	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1108793	AGCCTTGACACCCCC[A/G]GGCTCAACAGTCTTC	285498
rs549751255	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1100945	TGTTATAGCTGTTCA[C/G]ATGGAATTCTGCGGC	285498
rs549772947	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RNF212	GRCh38.p7	4:1056354	ACATGCTGGTGGGCA[C/T]GAAGGCTGGAGGACT	285498
rs549811167	snp	A/C/T	0.00199529	0.0315338	intron-variant	RNF212	GRCh38.p7	4:1105682	TGAAACTGATTTCAC[A/C/T]GAAGTGCTCACACAC	285498
rs549838013	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1079458	AGGCAGAACAGGAGC[A/G]TTCTCATGACCCAGC	285498
rs549888138	snp	C/T			utr-variant-3-prime, intron-variant	RNF212	GRCh38.p7	4:1072367	AACCCATAGAACATT[C/T]GACACCTAGAGTGAA	285498
rs549918350	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1110938	GCAAACCTGTGAATC[C/T]ATACCTGCCCCAGGC	285498
rs549954861	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1078967	ACACAGGACCAACAT[A/G]GGACCAACACAGGGT	285498
rs549964642	snp	A/G	0.0228947	0.104514	intron-variant	RNF212	GRCh38.p7	4:1095894	TGGTCTCAGCATAGC[A/G]CACCTGGCTCATCAC	285498
rs550120996	in-del	-/A			intron-variant	RNF212	GRCh38.p7	4:1103268	TTAAAATCTTTGCAC[-/A]AAAAACTTACTGGGC	285498
rs550232095	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1057428	TATGCAGCAGACGGA[A/G]TGGGAGGCCACCCAG	285498
rs550264131	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1103754	TTAAAAAAGAAACCT[C/T]AGCAAAAACTTGATG	285498
rs550266940	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1095517	CAAGCACAACTCCCA[C/T]AGCTCCATGGTCTCG	285498
rs550291719	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1103070	TGTTAAACAAGAGGC[A/G]TCATTATGGAACTTA	285498
rs550344170	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1061703	GGACATCTCAGCTCA[A/G]CAAGAAAAGAGCAGA	285498
rs550370196	snp	G/T			intron-variant	RNF212	GRCh38.p7	4:1107742	GGCATGAGCCATCAC[G/T]CCCGGCAGGACTTAC	285498
rs550424853	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1097598	CAAAAGAAACAGCAT[G/T]TGGTTACAAGCCCTC	285498
rs550464170	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1085632	GCTGCTCTCCCAGGC[A/C]CCTCCCACTGCCTCA	285498
rs550466069	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1080104	CTGCCTGGCCACACA[C/T]ACCACACCGTGCACG	285498
rs550508142	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1088522	AACAAAATTGCAGCG[C/T]GACCATGCAGTAGAA	285498
rs550529227	snp	A/G	0.00318978	0.0398085	intron-variant	RNF212	GRCh38.p7	4:1085046	GGCACCTGCACACAC[A/G]CTGGAGGCTCACCCA	285498
rs550576894	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1102539	ATCCTGGCTAACAGG[A/G]TGAAACACTGTCTCT	285498
rs550603171	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1070736	GGTTTTGTAAGACTG[G/T]GTTCTTGGTTTTTAG	285498
rs550673924	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1061728	AGCAGAAACCATGAG[C/T]GGACACATCTGCGGC	285498
rs550681330	snp	A/T	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1064974	GCGTGTGCCAGAGTT[A/T]CCTTCCATTTTAAGG	285498
rs550693972	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1077486	GATCCACCTGCCTTG[G/T]CCTCCCAAAGTGCTG	285498
rs550725336	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1066522	TTTTGTAGAGATGGG[A/G]GTTTCACCATGTTGC	285498
rs550731150	snp	A/G	0	0	intron-variant, missense	RNF212	GRCh38.p7	4:1093455	CACACAGCTGCGGGA[A/G]AACTCCACCCTGCGT	285498
rs550783490	snp	A/T			intron-variant	RNF212	GRCh38.p7	4:1082375	ATGCACACGTAAGAC[A/T]GGGGGAGCGTGTCTG	285498
rs550793676	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1064278	GGAGCAATGTGGTTA[C/T]GTTCCACTGGAATTC	285498
rs550849812	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1088946	GGAAATGCCTGGATG[C/T]CCAGGCAGAAGTCTG	285498
rs550863596	in-del	-/TTTT			intron-variant	RNF212	GRCh38.p7	4:1083960	ATTTTTTTTTTTTTT[-/TTTT]GAGAGACGGAGTTTT	285498
rs551033472	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1074983	CATCACCGTCCCTTC[A/G]AACTACATTCCATTT	285498
rs551036654	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1060297	CCTGCCGATCAGCCC[A/G]CTGTGTGTCCCACAG	285498
rs551064294	snp	A/G/T			intron-variant	RNF212	GRCh38.p7	4:1106157	GGAAGACCAGCATTC[A/G/T]GAAGACACTGCGGAA	285498
rs551172258	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1075456	GCGTTGCAGGGCGAG[C/T]AGGCAAGAGACTGGG	285498
rs551242886	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1110161	GAAATCACGTGCGGC[C/G]AAAAGACAAAGGGAT	285498
rs551244442	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1068909	AACCTCTGAACAAAA[C/T]AGAAATCTATGAATA	285498
rs551244861	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1104366	TCAAGACCAGGCTCA[C/G]TGGGTGGCCTTCCAT	285498
rs551266688	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1066623	AGTGTGCACCACTGC[A/G]CCCAGGCTTTGCCCA	285498
rs551340346	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1091970	CAGCTCTTGTGCACA[C/T]TGCAGGCCATGGCCA	285498
rs551347974	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1079556	TGTCTACTGTTGCAC[A/G]AGAGGTTACGTTTTT	285498
rs551388450	snp	C/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1102060	AATACATATACTGCA[C/G]GCAAAAATGAACACA	285498
rs551415737	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1086282	AGCACCTTCCATACA[C/T]GGCCACTGCCAGCTC	285498
rs551525476	snp	A/G	0.0197687	0.0974348	intron-variant	RNF212	GRCh38.p7	4:1096618	CACCTGGCTCATCAC[A/G]GAACCAAGCACACCC	285498
rs551628386	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1112637	CAGGCGGACCCGCAG[C/T]CTGCAAGCCAGAGCC	285498
rs551667441	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1107642	TTTTTAGTAGAGATG[C/G]GGTTTCACTGAGTTG	285498
rs551674481	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1081350	GAGGGGGTGGGGTTG[A/G]GATGGGAAGGCAGGT	285498
rs551808720	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1089499	GATGAGATTTTGGGC[C/T]TGGACTTCTGAGTTT	285498
rs551820200	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1076365	TGGCGCTGGCTTTGC[C/T]TCTCCGAGTCCACCC	285498
rs551868217	snp	A/C	0.000399281	0.0141238	intron-variant, synonymous-codon	RNF212	GRCh38.p7	4:1094300	TCCTGGCAGCTTTCC[A/C]CCAGACTGGTGGACT	285498
rs551888883	snp	G/T			intron-variant	RNF212	GRCh38.p7	4:1063813	CAGGAGGTCCAGGCT[G/T]CAGTGAGCCATGGTC	285498
rs551949718	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1084669	TTGGGAGGTTGAGGC[A/G]TGAGCTGAGATCACG	285498
rs552022476	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1076827	TTTATTAGAACACAG[C/T]CATGGTCATGCCTAT	285498
rs552061570	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF212, LOC105374344	GRCh38.p7	4:1114223	GCACGGGAGGCCTGA[C/G]CCTGCTTCCCTCTGA	285498
rs552105999	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1099097	ACAGCACAGATGCAC[A/G]GACCTCAGTGAGGCC	285498
rs552112228	snp	A/G	0.00318978	0.0398085	intron-variant	RNF212	GRCh38.p7	4:1095540	TGGTCTCGGGATAGT[A/G]CACCTGGCTCATCAC	285498
rs552145955	snp	C/T	0.00398564	0.0444627	intron-variant	RNF212	GRCh38.p7	4:1059828	GGCTGGGTGTGGTGG[C/T]TCATGCCTGTAATCC	285498
rs552161096	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1078894	AGGACCGACATGGGA[A/C]CAACACAGGGTCAAC	285498
rs552181788	snp	A/G	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1110889	TGCACTCAGACTACT[A/G]GAATCTGTGTTGACC	285498
rs552332962	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1076986	TGTAATCCCAGCACT[C/T]TGGGACGCTGAGGTG	285498
rs552338391	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1083158	TCAGCAGAAATATAC[C/T]TCCCTCCAGCGAGAG	285498
rs552391968	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1105624	ACATGAGACTGGAAA[C/T]CATCAGAGGGTACTG	285498
rs552446170	snp	C/T	0.0023933	0.0345097	intron-variant	RNF212	GRCh38.p7	4:1102053	ATCATCAAATACATA[C/T]ACTGCAGGCAAAAAT	285498
rs552479590	snp	A/G	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1078485	CTGAGTTCCGGGCAG[A/G]TTTCCTCTGGTCTTG	285498
rs552535348	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1100790	ATGGCTGAATTTTAC[A/G]TCAGAAATTAGATGA	285498
rs552626106	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1061224	GCTGCTCCACCTCCC[C/G]CTACCCCACTCTACC	285498
rs552704643	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1062604	ACAAAGACAAGGATG[C/T]CTGTTCTTGCCGCTT	285498
rs552719111	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1101682	GAAACCTCTACTGAG[C/T]GTCATCCCTCCTCCA	285498
rs552752103	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1067031	CCAGTTTTCCCAACA[A/C]CATTTCTCAAAAAAA	285498
rs552785055	snp	C/T	0.260227	0.249791	intron-variant	RNF212	GRCh38.p7	4:1095466	ACTCCCACAGCTCCA[C/T]GGTCTCGGGATAGCG	285498
rs552854646	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1091172	CCTGACCAAACAGGT[A/G]TGGACCAATGGCTGG	285498
rs552921911	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1090687	TATTGCATCTAGCAG[C/T]CATCCCCTTTGAGAG	285498
rs552972960	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1096381	GCACCTGGCTCATCA[C/T]GGAACCAAGCACACC	285498
rs553071585	snp	C/G	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1063281	AACAAAGTTGGAAAA[C/G]TCACACTTCATAATT	285498
rs553086205	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1070253	GTGGGTGGTTTTGTA[A/G]GACTGTGCTGTGTCA	285498
rs553108108	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1091711	AGGCCTTTGTTCCCA[A/T]CCTCCTCCATGAGAG	285498
rs553167061	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1064030	AAATATGGAAAAAAA[A/C]AATGAAGAGAACTGA	285498
rs553181067	snp	C/T	0.00159617	0.0282053	intron-variant	RNF212	GRCh38.p7	4:1102808	AGTGAGCCAAGACTG[C/T]GCCACTGCACTCCAG	285498
rs553184111	snp	A/G	1.64928e-05	0.00287161	synonymous-codon, intron-variant, nc-transcript-variant	RNF212	GRCh38.p7	4:1081427	CACACACCTGTCGGG[A/G]GCTGATGAGTGAGGT	285498
rs553242756	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1092050	GGGAACACCTGCACA[C/T]GCCCCTCAAAGCCAC	285498
rs553257994	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1098305	TAGAAAACAGGAAAT[C/G]ATATCTTGAATTGAC	285498
rs553272163	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1083201	AGGCAGATTTGGATT[C/T]CTGAGGATATCAGGT	285498
rs553339920	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1078708	GAGACTGACAGGGAC[C/T]AGCACGGGACCAACA	285498
rs553356607	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF212, LOC105374344	GRCh38.p7	4:1114404	TTGTGCCGGGAGAGC[A/G]CAGGGTGAGCGCTCC	285498
rs553416101	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF212, LOC105374344	GRCh38.p7	4:1113952	GGCGAGGCAGGGGAG[G/T]AGTAGGGGAGAGTGG	285498
rs553557947	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1103225	CTTTAAACAGTTCGA[C/T]GTCTAATAAAGATAT	285498
rs553640104	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1094955	AAATGTTTCACCATT[A/G]AGAAAGTAAAAATTC	285498
rs553682462	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1110516	TGTCTCATAGCAAAA[C/T]GGCAGAAACTATGTT	285498
rs553715730	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1105369	TCTGCTCTGCTCCCT[C/G]GCCATCCACCACCCA	285498
rs553789886	snp	C/T	0.00358779	0.0422022	intron-variant	RNF212	GRCh38.p7	4:1095571	AGAACCAAGCACACC[C/T]CCCACAGCTCCATGG	285498
rs553834666	snp	G/T			intron-variant	RNF212	GRCh38.p7	4:1107921	TATACCAATAACAAG[G/T]TAAACTGAATATTTT	285498
rs553899918	snp	A/C	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1112151	GGCGGAGGCTGCAGT[A/C]AACCGAGATCCCGCC	285498
rs553961522	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1111812	AGTAGCATTATTTCT[A/G]CAGCCAAATCTGCAA	285498
rs553986928	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1084451	AAAATACATTGTGGC[C/T]GGGTGCAGTGGCTCA	285498
rs554087204	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1057174	GCAGAAGATGTGGAC[C/T]GATGCTGCAGGGCCC	285498
rs554090403	snp	A/T			intron-variant	RNF212	GRCh38.p7	4:1090449	GACTTGTTTTTCAAA[A/T]TGGGATGGTTGAGCA	285498
rs554113228	snp	A/G	0.00199481	0.0315187	intron-variant	RNF212	GRCh38.p7	4:1083971	TTTTTTTTGAGAGAC[A/G]GAGTTTTGCTCTTGT	285498
rs554124880	in-del	-/ATGGGACCAACAT	0.0189856	0.0955633	intron-variant	RNF212	GRCh38.p7	4:1079031	CAACACAGGACCAAC[-/ATGGGACCAACAT]AGAGTCAACACAGGA	285498
rs554148244	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1061366	ATCTGCAGGACCTGG[A/G]GAGGCCCACAGTCCT	285498
rs554176184	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1090500	TCCAAACTCCCAAGG[C/T]CCCAGTGTTGCCCCA	285498
rs554190520	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1085143	AGCCAGCAAACGGGG[C/G]CTTGTGACTATTCAA	285498
rs554210099	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1091809	TTTCCTGGCTGCTGC[A/G]TCCTCGGAGTGACTT	285498
rs554254934	snp	G/T	0.0333695	0.124785	intron-variant	RNF212	GRCh38.p7	4:1087377	AGGATGGGGTGGGGG[G/T]GAGAGGATGGGGTGG	285498
rs554258774	snp	C/G	0.000399281	0.0141238	synonymous-codon, intron-variant, missense, nc-transcript-variant	RNF212	GRCh38.p7	4:1079664	AATCGGAGAAGGAGA[C/G]AGATCAACTTCCATC	285498
rs554292731	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1105961	GCTGCCTGGGGACCA[A/C]GAGGCGGCCAGAGGC	285498
rs554322498	in-del	-/GA	0.00159617	0.0282053	intron-variant	RNF212	GRCh38.p7	4:1076503	TGGGAGGTTCACCTC[-/GA]GAGAGGCCTGCACAC	285498
rs554405738	snp	A/C	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1074542	CTCTACCAGCACAGG[A/C]GTGCCCTGCTCCAGG	285498
rs554428572	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1078490	TTCCGGGCAGGTTTC[A/C]TCTGGTCTTGCTTCT	285498
rs554484023	snp	A/G	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	RNF212, LOC105374344	GRCh38.p7	4:1114576	ATATATATCAGTAGC[A/G]TTGATTTTACCCTTT	285498
rs554485223	snp	A/C	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1068273	AGAAAATATACTCAT[A/C]GACAGGGTCCGGAAG	285498
rs554485681	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1069997	GTTTTGTAGGATTGC[A/G]CTGTGTCAGCGTGGA	285498
rs554534153	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1093014	CGTGCTCAGTGCTGA[C/T]GCAGCCTGTGGTAGG	285498
rs554542736	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1075113	TGCAAACCTTTCTTG[G/T]AAATGGGCCATGGCA	285498
rs554592528	snp	G/T	0.000399281	0.0141238	downstream-variant-500B, intron-variant	RNF212	GRCh38.p7	4:1071039	TTTTAAAAAACTAAT[G/T]TTTTTAAATACTGTT	285498
rs554673289	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1087965	TTTATAAATCACCCA[A/G]TCTCAGGTAGTTCTT	285498
rs554760612	snp	A/G	0.00119737	0.0244387	downstream-variant-500B	RNF212	GRCh38.p7	4:1055961	GGTGAGCTCAGGCCC[A/G]GAATTCATCTCTGGA	285498
rs554769483	snp	C/T	0.000399281	0.0141238	intron-variant, missense, downstream-variant-500B	RNF212	GRCh38.p7	4:1093611	GCTGGAGGGGCTGGC[C/T]GGGTCTGCTGGGTCT	285498
rs554805324	snp	A/C	0.00318978	0.0398085	intron-variant	RNF212	GRCh38.p7	4:1078247	TCACCGCCGCCAGAA[A/C]ACACTCAGTTTTCCT	285498
rs554821313	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1082658	GACAGCCTGTGTCCC[A/G]GCCCGACATACAAGT	285498
rs554840440	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1109244	AACTCCTGACCTCAG[A/G]TGATCAGCCCACATC	285498
rs554856375	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1082980	CAAAAGTGGGTGGCA[C/T]GAACGCCACCACAGT	285498
rs555010438	snp	C/T			intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1073217	AGATGCAGGAGACAG[C/T]GTGTGGGGAGATGGC	285498
rs555032316	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1103973	GGCGTATGTAAATGT[C/T]CTAGCAGAATCTACA	285498
rs555072125	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1068195	GTTAGAGGGCTATGC[C/T]GTCTAATTCCAAAAC	285498
rs555086009	snp	C/T	0.00199481	0.0315187	intron-variant	RNF212	GRCh38.p7	4:1061873	AGTACCCAGGTTGTC[C/T]AGATTGCAGCCCCAA	285498
rs555109624	snp	C/T	0.00119737	0.0244387	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1058287	TTGCGGGGGTTAGAA[C/T]GCAGTGAAGAAGGTG	285498
rs555192134	in-del	-/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1058996	CTTTCTCCAGGCGCC[-/T]TGTAACATGAAAGGG	285498
rs555202549	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1080232	GGCTCGTGATCTCTG[C/T]GGAAAGAGGCTCACT	285498
rs555209363	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1090123	GGGGTTGGGGTGACA[A/G]GACAGGGATGGGGTA	285498
rs555229965	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1075034	TCTCCGCAGAGCGTT[C/G]AAGTGCTGGTGTCTT	285498
rs555260045	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1091595	CTGCGATGATAACAC[A/G]AGCAGGAGGGAGCGG	285498
rs555263892	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1085315	TACGGCAAAAGCACG[C/G]ATGAGCTAAAATGTA	285498
rs555322909	snp	A/C	0.00199481	0.0315187	intron-variant	RNF212	GRCh38.p7	4:1096289	ACACCCCCCACAGCT[A/C]CACGGTCTCGGGATA	285498
rs555373496	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1101201	ACGACTGGCACTCAC[A/C]GTGCAGTAGCCGTGG	285498
rs555436931	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1105757	GTCCTTCCACCGCAG[A/G]TCAGGGTCAAAGAAG	285498
rs555450807	snp	C/T	0.00398564	0.0444627	intron-variant	RNF212	GRCh38.p7	4:1095708	ACAGCTCCATGGTCT[C/T]GGGATAGCGCACCTG	285498
rs555478832	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1065721	CTTCCCAAGTAGCTG[C/G]GACTACAGGTGTGTG	285498
rs555512057	snp	A/G	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1102738	GCCCCTGCAGTCCCA[A/G]CTACTCGGGAGGCTG	285498
rs555569744	snp	C/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1102436	GATCTGCATCTGACT[C/G]GAAAAATCTCTATGT	285498
rs555570600	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1107286	TCGATCTCCTGACCT[C/T]ATGATCCGCCTGCCT	285498
rs555608983	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1076017	TGTATTTGTGAGTCA[C/T]GATTTTACCTTTTCA	285498
rs555651441	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1097326	CAGCGTCTCGTAGGT[C/T]GGGAGCGGTGGCTCA	285498
rs555719638	in-del	-/AT	0.350109	0.229081	intron-variant, frameshift-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1093541	GGCAGAGCCTGTGAC[-/AT]CTCCACGGCCCATGC	285498
rs555734139	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1082919	CAACTCTAAAATGCA[C/G]TGTTTCGTGGGAGCA	285498
rs555834199	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1110021	TAAGTGCAAATTCTG[C/T]AGCAAGAAAATTCCT	285498
rs555880584	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1088937	AAGATGTATGGAAAT[A/G]CCTGGATGTCCAGGC	285498
rs555909881	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1104909	AAGAACACAGGTGCA[C/T]GTCATGAGGCATTTG	285498
rs555931830	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1070164	ACTGCGCTGTGTCAG[C/T]GTGGACGCCTGGCCT	285498
rs555953746	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1078640	GACAGCAAGTGAAGG[C/T]AGTTAAAGCCCAGGG	285498
rs555972975	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1104597	AGAAAGGGAGCAGGC[A/G]TGGTGATGACTGCCC	285498
rs555997977	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1063534	TGGCCAACATGGTGA[A/G]ACCCCATCTCTACAA	285498
rs556008573	snp	G/T	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1103942	CTAAAGCGTCCTTAT[G/T]CAAAGATAACATGTT	285498
rs556030582	snp	C/G	0.00398564	0.0444627	intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1111975	CACATTTCGGGAGGC[C/G]AAGGCCGGTGATTGT	285498
rs556075915	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1058930	ACCCTGAGAACTGCC[A/G]GAAGGGCAAAAGCGC	285498
rs556090389	snp	A/G	0.000979647	0.0221103	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1073218	GATGCAGGAGACAGC[A/G]TGTGGGGAGATGGCC	285498
rs556139013	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1063968	AAGTCAACCAAGAAA[A/G]TGTATCTTCAGTGAA	285498
rs556253767	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1078178	TGTGTCGCACAACCC[A/G]AAGCAACACATAAAT	285498
rs556266265	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1095182	TCCATGGTCTCGGGA[G/T]AGCGCACCTGGCTCA	285498
rs556298094	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1062597	GAACAGAACAAAGAC[A/G]AGGATGTCTGTTCTT	285498
rs556324428	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1070451	GCCTGGCCTGAGTTA[C/T]GGGTGGTTTCGTAGG	285498
rs556338837	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1069841	ATGTTCCAGTCCAGA[A/G]GAGAGAGAAGAGATG	285498
rs556429229	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1057150	ACGCACACCCCCGCC[C/T]GGCGGCCAGCAGAAG	285498
rs556475470	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1060853	AACGCACAGATGGCC[C/T]GCCTGCCACTCCAGC	285498
rs556531942	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1111061	CACACGCGTCTCCAT[C/T]ATTCCTAACAATGTT	285498
rs556535761	snp	G/T			intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1112112	CCCTGGAGGCTGAGG[G/T]AGGAGAATCACTTGA	285498
rs556547213	snp	C/T	0.00159617	0.0282053	intron-variant	RNF212	GRCh38.p7	4:1074447	CCTGGCTTCTGCCCC[C/T]GGCACAGCCACCCCA	285498
rs556570196	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1094801	AACCTGAGATTCTAA[C/T]GTGTGAATATGGGGA	285498
rs556652813	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1083819	GTGGCTGGGGATGCA[A/G]AGGGTACTACTTGAA	285498
rs556690062	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1058443	ATGTTAACACATCAC[A/G]GTGCTTTGAGGACGA	285498
rs556713575	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1079225	GAGTCAACACAGGAC[A/C]AACATGGGACCAACA	285498
rs556769720	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1077601	AAGGTAGAAAGCTGA[C/T]CTGACAGAACAAAGT	285498
rs556791865	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1084383	GTCTCCGTTGCAATG[C/T]GTTTACAATCTTCTA	285498
rs556834335	in-del	-/A	0.00755907	0.0610114	intron-variant	RNF212	GRCh38.p7	4:1089605	GATTTGGGAGGGGCC[-/A]GGGGTGGAATGATGT	285498
rs556844406	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1073884	CTGATTACCTGTTTG[A/T]TTCCCTCTGTTCCAC	285498
rs556899628	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1097166	CCTCCAGCCCAGCCT[C/T]CTCCTTTAGTATGGA	285498
rs556928746	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1105852	GATGGAGCCTGTGGC[C/T]ATCTGGGAGGACATT	285498
rs556930460	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1079579	ACGTTTTTCACTACT[A/G]AGGAAAATGGGAAAT	285498
rs556931612	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1070947	CGAAATAAATTATTT[A/T]AAAAAACTAATTTGT	285498
rs556965045	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1102664	GAGACCATCCTGGCT[A/G]ACATGGTGAAACCCC	285498
rs556982518	in-del	-/T			intron-variant	RNF212	GRCh38.p7	4:1066090	ATACTATCTTGCTGT[-/T]TTTTTTTTTTTCTCT	285498
rs557003524	snp	A/T	0.00398564	0.0444627	intron-variant	RNF212	GRCh38.p7	4:1063883	TCAAAAAAAAAAAAA[A/T]GAAAAAAACCAATAT	285498
rs557052314	snp	A/G	0.0352966	0.128072	intron-variant	RNF212	GRCh38.p7	4:1086745	AGAGAGGATGGGGTA[A/G]GGGTGAGAGGATGGC	285498
rs557063871	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1058835	TGGGCATGCGGACTG[G/T]GCCTGGCATACACAG	285498
rs557176660	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1077099	CAGGCATGGTGGTGC[A/G]TGCCTGTAGTCCCAG	285498
rs557181908	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1097750	CAGCTGTCCTAGGCA[C/T]GGAGCTGCCGTGAGC	285498
rs557187828	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1087906	GTAAGTTTCCTGAGG[C/T]CTTCCCAGCCATGCA	285498
rs557191043	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1082547	GGAATAGGCAGTTGC[A/G]CAACAGCTCAACCAC	285498
rs557240058	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1081819	CTAGCGCTGAAGCCA[A/G]GTGAACTCAACACCC	285498
rs557252720	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1088718	GCCAAGGCCCCCTGC[C/T]CAACTCTCGTGCAGC	285498
rs557272328	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1064413	ACAGGAGAACTAAAA[C/T]GTGTATTAGTCTGCT	285498
rs557327981	in-del	-/T	0.00716266	0.059414	intron-variant	RNF212	GRCh38.p7	4:1107616	ACCACGCCCAACTAA[-/T]TTTTTTTGTATTTTT	285498
rs557356529	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	RNF212	GRCh38.p7	4:1055915	CTCCTGACGGATGAG[A/G]AGGCTCCACCCACGC	285498
rs557367402	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1103358	AAAAATTTTCCAGAG[A/G]AGAGAAAAATAAAAA	285498
rs557390624	snp	C/T	0.000735564	0.0191635	intron-variant, synonymous-codon, downstream-variant-500B	RNF212	GRCh38.p7	4:1093937	TTGGCTTCCATGGGT[C/T]GAGCCTCTGGGCACC	285498
rs557402252	snp	A/G	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1068033	AAAACTGTGAAGATG[A/G]CAATTCTCCCCACAC	285498
rs557412506	snp	C/G	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1064528	ATCAAGATGCTGGCT[C/G]ATGGGGGTCCTGGCT	285498
rs557452872	in-del	-/CAAA	0.00557542	0.0525036	intron-variant	RNF212	GRCh38.p7	4:1077229	AGTGAGACTCTGTCT[-/CAAA]CAAACAAACAAACAA	285498
rs557461318	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1077445	ACTATGTTGCCCAGG[C/G]TGGTCTTAAACTCCT	285498
rs557461855	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1067368	CAAAATTAATAATTA[C/T]ATAAAATATCAATGG	285498
rs557463799	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1074314	TTCCTGGGCTCGCTC[C/T]TCTGGCTCTCCACTC	285498
rs557479113	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1080831	TGAATTTGTGCCTTC[A/C]ATCTGAAGAGCTAGG	285498
rs557496720	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1085151	AACGGGGGCTTGTGA[C/T]TATTCAACGCGTCTC	285498
rs557540063	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1059967	GGCGTGGTGGCGCAT[A/G]CCTGTAATCCCAGCT	285498
rs557576714	snp	C/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1098530	CAACAGAGGGGAGAC[C/G]TGGCTCTGGCTCGGA	285498
rs557634920	snp	A/G	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1090957	CAGTGCTTGTCTTAC[A/G]TGTGTCCTGCCCCCA	285498
rs557635119	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1095628	ACAGAACCAAGCACA[C/T]CCCCCACAGCTCCAT	285498
rs557710508	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1085295	TGTATTCAGAACAGA[C/T]GCAATACGGCAAAAG	285498
rs557715017	snp	C/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1101176	TGCGACCCCTAGACC[C/G]ACGGGCCTAACGACT	285498
rs557771815	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1091492	CCAGGCTGGAAGGGC[C/T]GACAGACAACAGGGC	285498
rs557824214	snp	C/G	0.0023933	0.0345097	intron-variant	RNF212	GRCh38.p7	4:1111095	TTCGGGGAACATTAT[C/G]TTGGGTCACCAGTGC	285498
rs557827150	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1112172	AGATCCCGCCACCGA[A/G]CTCCAGCCTGGGCGA	285498
rs557844030	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1100656	TCAGGTGATCTGCCC[A/G]CCTCGGCTTTGCAAA	285498
rs557964438	snp	C/G	0.00676609	0.0577691	intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1113288	ACCCAAGTCCCCCAT[C/G]CCCCGGAGTTCCCTG	285498
rs557966617	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1106849	ATATCTTTTGCCCTT[A/G]CTTTTTCATTACTTC	285498
rs557988374	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1080209	CCTCCTAGCCCTGCC[A/G]TCCTTATGGCTCGTG	285498
rs558018836	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1058002	GGAGGCGGAGGTTGC[A/G]GTGAGCCAAGATGGT	285498
rs558036824	snp	C/T	0.0023933	0.0345097	intron-variant	RNF212	GRCh38.p7	4:1096062	ACAGCTCCATGGTCT[C/T]GGGATAGCGCACCTG	285498
rs558173021	snp	C/T	0.000388878	0.0139387	intron-variant, missense, downstream-variant-500B	RNF212	GRCh38.p7	4:1093557	CTCCACGGCCCATGC[C/T]GGAAGCCTGAGAGGC	285498
rs558175784	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1084585	AAATAAAAAAATTAG[C/T]TGTGTGTGGTGGTGC	285498
rs558177678	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1102370	CCTGCATACAGGAAA[C/T]GTCAGCCCTCCATCT	285498
rs558186455	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1080711	GAGCCTTCTTTCCTG[C/T]CTCTTGCTACCTGTG	285498
rs558222358	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1096709	TCATAGCTCCATGGT[C/T]TCGGGATAGTGCACC	285498
rs558230002	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF212, TMED11P, LOC105374344	GRCh38.p7	4:1115412	TTTCTTCACGGTCCT[A/G]TGCGGAAAAGAAGTA	285498
rs558283210	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1109859	TCAGTGTCCGCAGCT[C/T]CCAGCACACAGAATG	285498
rs558322392	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1082827	GCTGACTGTGGTGGG[C/T]GGAAGTACCTGAGCC	285498
rs558325245	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1075961	GGTACTGTGTCTGGC[C/T]ACCTCATAAGTTGAA	285498
rs558329704	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1062004	CTCCAGAGCGGCTAC[C/T]GTAAATGAGCCAAAG	285498
rs558344618	snp	A/G	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1109260	TGATCAGCCCACATC[A/G]GTCTCTCAAAGTGCT	285498
rs558482936	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1075506	TAACCAGCCAGATCT[C/T]GTGAGAACTCACCCA	285498
rs558505058	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1088644	AGGGCATGTGAGAGA[G/T]CTTCACAGCAGCCCC	285498
rs558521413	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1067087	TCTTTCTCCATTGAA[C/T]AGTGTGTTTTGTTTT	285498
rs558522148	snp	C/T	0.00478085	0.0486577	intron-variant	RNF212	GRCh38.p7	4:1069547	CCTGGAGGAATCAGG[C/T]GACCAAGGTGAACAT	285498
rs558558075	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1106532	TAAAAAAATAAAGAC[A/G]TATTAGAGATTATTT	285498
rs558644713	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1077704	GACAGCTGGAAGCAG[A/G]TGTCTGGCCTTGGGG	285498
rs558671544	snp	A/T	0.000399281	0.0141238	downstream-variant-500B	RNF212	GRCh38.p7	4:1055989	GGACCTGACGGAGAT[A/T]CACCCGCTGAAGCCG	285498
rs558692656	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1066561	GTCTCGAACTCCTGA[A/G]CTCAAGCGATCCTTT	285498
rs558708918	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1104846	CATCTAATGGCGGCA[C/T]GGGGCAGGACAGCTA	285498
rs558742754	snp	A/G	0.00279162	0.0372561	intron-variant	RNF212	GRCh38.p7	4:1082926	AAAATGCACTGTTTC[A/G]TGGGAGCAAGAGGAT	285498
rs558783321	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1078093	TGTGATTACCCATGC[C/T]ACAGGGCTGCTACAC	285498
rs558783467	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF212	GRCh38.p7	4:1071924	ACTCCTTAGTATTTA[C/T]CCAAAGGAGCTGAAA	285498
rs558829118	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1069778	CTTCAGAATTTGAGG[C/G]CTTTATTCTTCGGAA	285498
rs558833760	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1060805	ACAGGTCAGACAGCC[C/T]CACACACTGCTCAGT	285498
rs558927860	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF212	GRCh38.p7	4:1072496	GGGGAGCTGTGCGTG[C/T]GTGGAGTCATGGTGT	285498
rs558939919	snp	A/C/T	0.0017885	0.0298584	intron-variant, missense, downstream-variant-500B	RNF212	GRCh38.p7	4:1093986	GGGCATAACTTGAGA[A/C/T]GGCAACAGCCTCGGG	285498
rs559002007	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1083783	GCAGAGGCTGACGTC[A/G]AGGGTGGGGAGCTGC	285498
rs559097438	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1094669	CATGCAGGGCTCAGC[A/G]GGGATTGGAGGCCTG	285498
rs559105744	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1074937	CGCTAGGATGTCTTC[A/C]ATATCAAGTTCATCC	285498
rs559186579	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1058982	CCCACCCGTGTTTGC[C/T]TTCTCCAGGCGCCTT	285498
rs559218113	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1077131	TACTCGGGAGGCTGA[A/G]GCAGGAGAATTCCTT	285498
rs559239175	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1089704	CGGTGGGAAGTGATT[A/G]GATCATGGGGGCAGT	285498
rs559245063	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1075345	AGGTTTAACTGGCTC[A/G]TGCTTCTGAGGGCCG	285498
rs559331407	snp	A/C			utr-variant-3-prime, intron-variant	RNF212	GRCh38.p7	4:1072377	ACATTCGACACCTAG[A/C]GTGAACCCTAATGTA	285498
rs559344442	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1059884	TGGATCACCTGAGGT[C/T]GGGAGTTCAAGACCA	285498
rs559347018	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1069128	AGGCACAAGAATCGC[C/T]TGAACCTGGGAGGCA	285498
rs559412777	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1096947	TATAGATGACTCAAG[C/T]GGCCAGCACATTGTG	285498
rs559421862	snp	A/C	0.00159617	0.0282053	intron-variant	RNF212	GRCh38.p7	4:1095810	ACCAAGCACACCCCC[A/C]ACAGCTCCATGGTCT	285498
rs559521027	snp	A/G			upstream-variant-2KB, nc-transcript-variant, intron-variant	RNF212, TMED11P, LOC105374344	GRCh38.p7	4:1115407	AAAATTTTCTTCACG[A/G]TCCTATGCGGAAAAG	285498
rs559659847	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1086179	GCCCCAGGGGACAAA[C/T]CTCAGTGCTGCACCC	285498
rs559723166	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1112490	AACACAAAATTTTCA[C/G]AGAAAGAAAAACGCC	285498
rs559860091	snp	G/T	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1058670	ATGCACCTCTGCAGC[G/T]TAGAGAATATGTAAG	285498
rs559865803	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1073731	GATTCGGACTCCCAC[C/T]GTCTGTTAGGAACAC	285498
rs559867847	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	RNF212	GRCh38.p7	4:1055909	CCCACCCTCCTGACG[A/G]ATGAGGAGGCTCCAC	285498
rs559878108	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1094888	GACACCAAAAGCAAA[A/T]ACAATAAAACAGACC	285498
rs559907179	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1110101	CGACTCATAAAAATC[A/G]AAAAGTTCTTACAAG	285498
rs559931253	snp	A/C			downstream-variant-500B, intron-variant	RNF212	GRCh38.p7	4:1071189	AAATTATTTTTAAAA[A/C]CTAAGTTGGTTTTTT	285498
rs559945748	in-del	-/C	0.00478085	0.0486577	intron-variant	RNF212	GRCh38.p7	4:1111014	CTATGACGCTCTGAG[-/C]CCTGTCTTCACACTT	285498
rs559999068	snp	G/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1087563	GGCTGACAGGACAGG[G/T]TGGGTGTGACAGGAG	285498
rs560091662	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1065785	AGAAACAGGTTTCAT[C/T]ATGTTGGCCAGGCTG	285498
rs560093927	snp	G/T			intron-variant	RNF212	GRCh38.p7	4:1107214	GTGCCACCATGCCCA[G/T]CTAATTTTTTGTATT	285498
rs560260287	snp	C/T	0.00835141	0.0640778	upstream-variant-2KB, intron-variant	RNF212, LOC105374344	GRCh38.p7	4:1114218	CCTCAGCACGGGAGG[C/T]CTGAGCCTGCTTCCC	285498
rs560299390	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1089163	CTGCAGGCACTCAAC[C/T]CCAGCCCAGAAAGCA	285498
rs560322358	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1099692	ACAATGGTACAGTAA[C/G]GAGGATACATAGTTA	285498
rs560323377	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1060215	AGGCCAACAATTCAC[C/G]CAGGGTCTGGCAAGC	285498
rs560323805	snp	A/C	0.00358779	0.0422022	intron-variant	RNF212	GRCh38.p7	4:1083572	GAACCCGGCAGGCGG[A/C]GGTTGAGGTGAGCTG	285498
rs560384202	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1057332	CTGGGGGGCTGACAT[A/G]GGAGGGTCTGCCTTT	285498
rs560399622	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1083118	ATGTAGAGAGTGGGA[C/T]TGGCCTGTGCAACCT	285498
rs560486703	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1078880	CACAGGGTCAACACA[A/G]GACCGACATGGGACC	285498
rs560532747	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1073976	AAATTTGCAGCTGAT[A/G]TTAGAGAATGTGAAA	285498
rs560582393	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1079331	CACAGGACCAACATG[A/G]GACCTGTACGGGAAC	285498
rs560590499	snp	C/T	0.000215312	0.0103735	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1073564	ATTTTAATCGATGCA[C/T]GTATCGGTCTGAGGT	285498
rs560612488	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1105220	GTGTAAAAACCGGCC[C/T]GGTCTAGCTTACACT	285498
rs560656562	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1061650	CACAGACAGAGCAGC[A/G]GCCAACCGCTGAGCT	285498
rs560773770	snp	A/G	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1070000	TTGTAGGATTGCGCT[A/G]TGTCAGCGTGGACGC	285498
rs560800210	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1107425	AACTCCTGGTCACTG[C/T]CATCTCTGGGAAACA	285498
rs560813502	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1059103	CAAGCATTAGGCTTC[C/T]CCAGCGCAGTGACTG	285498
rs560833535	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1076148	CCTTAGTCAACACTT[C/T]CATCTGCATGTGAAG	285498
rs560854697	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1081117	AGGGCTGTCAGCTGC[C/T]GGGCACTGGAACGCC	285498
rs560862073	snp	G/T	0.000798403	0.0199641	upstream-variant-2KB, utr-variant-5-prime, intron-variant	RNF212, LOC105374344	GRCh38.p7	4:1113579	CGCCTGCGCAAAGTC[G/T]ACGGCAGCCCTGCGC	285498
rs560876989	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1111086	AATGTTATCTTCGGG[A/G]AACATTATCTTGGGT	285498
rs560877003	snp	A/T			intron-variant	RNF212	GRCh38.p7	4:1092743	CAGCCCAGGGCCCCA[A/T]GGAAGAGCTGCCCGG	285498
rs560915915	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1076679	AAGGAACTGCTACAC[A/T]CATCCACTCCAGGGT	285498
rs560921748	snp	A/T	0.00279162	0.0372561	intron-variant	RNF212	GRCh38.p7	4:1070845	CAAAATGTTAACATT[A/T]GGGGAATCTGGACAA	285498
rs560989773	snp	G/T	0.000580648	0.017029	missense, intron-variant, nc-transcript-variant	RNF212	GRCh38.p7	4:1081582	TTGAAACTGAACTTT[G/T]TATTGTGCTGAAAGC	285498
rs560990504	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1064795	GAAACTCCCATTAAA[C/G]GAGAGCTTCCCACCC	285498
rs561018509	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF212, LOC105374344	GRCh38.p7	4:1114164	CAGGCCGCGCTGCAC[C/G]CTTTGGGACTAGTGT	285498
rs561020299	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1102937	ACGAGGTCAGGAGAT[C/T]GAGACCATCCTGGCT	285498
rs561099527	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1058511	ACTGCCTCCCTGCCA[C/T]GAGGGCAGTGGCAGG	285498
rs561125489	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1070462	GTTACGGGTGGTTTC[A/G]TAGGACTGTGCTGTG	285498
rs561127426	in-del	-/AAT	0.00159617	0.0282053	intron-variant	RNF212	GRCh38.p7	4:1082957	GATGACAAAAACAAC[-/AAT]GACAACAAAAGTGGG	285498
rs561148584	snp	C/T	0.00478085	0.0486577	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1056592	GTGTATTTTAAAAAA[C/T]TCAGATGTCATCTTA	285498
rs561154205	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1107877	TGCACATTTTGGAGA[C/T]CAGGCAGAGAAAAGA	285498
rs561158866	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1103550	GCTACCTTGTATCAC[C/T]ACAAAGTTGAATTTG	285498
rs561201867	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1095103	CCAAGCACACTCCCC[A/G]CAGCTCCATGGTCTC	285498
rs561263908	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1064287	TGGTTACGTTCCACT[A/G]GAATTCAGTCGGTGT	285498
rs561270671	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1077855	GCACCCATAAGGAAG[C/T]GTGTCCCTCTGGAAG	285498
rs561300855	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF212	GRCh38.p7	4:1093346	TTCATTTAAAAATAA[C/T]AATAAATCCATGATG	285498
rs561434520	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1088206	TAGTGATATGGATGG[C/T]GAAGTTCAGGCTGAG	285498
rs561469313	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF212, TMED11P, LOC105374344	GRCh38.p7	4:1115088	GATGAGGTGCCTAAT[C/G]TATCAAATTCAGAAG	285498
rs561532649	snp	C/G	0.00716266	0.059414	intron-variant	RNF212	GRCh38.p7	4:1084613	TGCGTGCCTGTGGTC[C/G]CAGCTACTTGGCAGG	285498
rs561542634	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1106595	ACAGAATAGCAGTGC[A/C]CAGAAAGACACGGAT	285498
rs561555401	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1104701	AGAGTGGAGCGCCCC[C/T]ACCACCACTGTCACT	285498
rs561602713	snp	A/G	0.00159617	0.0282053	intron-variant	RNF212	GRCh38.p7	4:1109630	TCCTGGGTATTTTCT[A/G]CCCCATTCCCCATGG	285498
rs561639043	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1090544	ATAAGTGTGGCCAGG[C/G]AGGGAGGCCCATGCG	285498
rs561670182	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1057290	GGGGTGGACTGGACT[A/G]CAGGCATCAAAAGCC	285498
rs561671555	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1079877	TTTAGGGCCACCCGC[C/T]GTCTGTACTGGGATG	285498
rs561701139	snp	C/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1100689	GCTGGGATTACAGGC[C/G]TGAGCCACCGCACCC	285498
rs561702204	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1101432	TCTGAAAGGTCCTGT[A/C]AACATGGTATTCCCT	285498
rs561758986	snp	A/G	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1095084	CACCTGGCTCATCAC[A/G]GAACCAAGCACACTC	285498
rs561785235	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1074791	TCAGGAGCTTTTGTC[C/T]CTGTACCTTCAGCCT	285498
rs561813659	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1111925	GTAGATGAACTACAG[C/T]TACATACAAATACAA	285498
rs561837978	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1101869	CATTATGATTCTGAA[A/G]AATTGACTGAGGTAT	285498
rs561964621	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1091038	GGGAGGCTTAATGGG[C/T]ATGATAGGAAAGTCT	285498
rs562102062	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1064605	GTGTGTGCAGAGTTA[A/G]TAAGCAAGCTCCCTG	285498
rs562106219	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1091893	GGGAAGACAGTCCTG[G/T]GTGCCACCCCGTGGG	285498
rs562126223	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1062743	TAAATAAAAGGCATC[A/G]TGGTTGGAAAGGAAA	285498
rs562131642	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1112192	AGCCTGGGCGACAAA[A/G]CTGAGCTCTGCCTTG	285498
rs562171406	snp	A/C	0.115438	0.210697	intron-variant	RNF212	GRCh38.p7	4:1096513	ACGGAACCAAGCACA[A/C]CCCCCACAGCTCCAC	285498
rs562189392	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1062232	GACACACAATTCCTC[A/G]ACAAAATACCAGCAA	285498
rs562257373	in-del	-/AAC	0.00318978	0.0398085	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1056693	ATTACTGCGTTTCTG[-/AAC]AACTAAGGCAAAACT	285498
rs562303290	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1086128	GACACTTAGGAAATC[A/G]GCCTTGGGGGCCATG	285498
rs562363239	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	RNF212, TMED11P, LOC105374344	GRCh38.p7	4:1115457	AAGTACTTAACTCAC[A/G]ATTTTGAGGGGAGGG	285498
rs562370189	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1085657	GCCTCAGCAATCACT[A/G]GGGCACCTGCCCCAA	285498
rs562407538	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1092208	ATCCCGGCTGTGGGG[A/G]TGCCTGGTCTGGCTG	285498
rs562442159	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1084374	CCACATAAGGTCTCC[A/G]TTGCAATGCGTTTAC	285498
rs562473772	snp	C/T	0.00119737	0.0244387	utr-variant-3-prime, intron-variant	RNF212	GRCh38.p7	4:1071994	CAGCTTAATTCATAA[C/T]TGCCAAAACTTGGAA	285498
rs562497349	snp	A/T	0	0	downstream-variant-500B, intron-variant	RNF212	GRCh38.p7	4:1071222	ATACTGTTCTTACAA[A/T]TTTTTCTGTGCTTGA	285498
rs562675797	snp	A/C/G	0.000921376	0.0214439	intron-variant, missense, downstream-variant-500B	RNF212	GRCh38.p7	4:1093720	TGTGATAACAGACAT[A/C/G]TTTTATGAACTCAAG	285498
rs562722684	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1108621	AATATGTACAAAAAC[A/G]GTGACCATAAAGATC	285498
rs562782889	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1088952	GCCTGGATGTCCAGG[A/C]AGAAGTCTGCTGCAG	285498
rs562804793	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1061093	AACACACTGACTCCT[A/G]AAATCCCGTTGCAGC	285498
rs562808751	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1067510	GGATGGAAAAAGATA[C/T]ACCATGTGAACTATA	285498
rs562820482	snp	C/T	0.02016	0.0983543	intron-variant	RNF212	GRCh38.p7	4:1095001	TTTGGCAGAAAATAT[C/T]TGCTGATCAAATATC	285498
rs562865803	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1087593	GCAGGGAGTGGGTAA[C/T]AGGATGGGGTAAAGG	285498
rs562910231	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1109483	CTGAACAAGCCCGGT[A/G]GCTTTGTCCCCTCCT	285498
rs562918406	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1089333	TGGGTTCTGGACTTG[A/C]ATGGGGCCTGCAGCC	285498
rs562958278	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1110667	ACACTATTGCTTTTG[C/T]TTTAAAAATCTGCAT	285498
rs563025930	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1105148	CTGGCGTGTCCATGA[A/C]TGTGGGGCATCCTCG	285498
rs563039696	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1067561	AAGAAAATCCCACCG[C/T]AAAAAATAATGAAAT	285498
rs563171041	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1105476	GATATCTCAGGTGGT[A/G]ACACACACTGCGAAG	285498
rs563208649	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1063573	AGGTGTGGTGGTGCG[A/C]ACCTGTAATCCCAGC	285498
rs563210675	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1070341	GGACGCCTGGCCTGA[C/G]TTACGGGTGGTTTTG	285498
rs563257008	snp	C/T	0	0	intron-variant	RNF212	GRCh38.p7	4:1085568	CGCAGTCCCTGGCTG[C/T]AGGGCCACCCCACCT	285498
rs563260370	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1080570	TGCCCTCAGTCACAG[C/T]GGGACCCCGTGGAGC	285498
rs563346269	snp	A/G	0.00199481	0.0315187	intron-variant	RNF212	GRCh38.p7	4:1064177	AATAATGACAACACC[A/G]TATTGTTAGATTTAT	285498
rs563353957	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1112951	CTCACTCCCCCGCTC[C/T]CTCCCCACCGCTTCT	285498
rs563512099	in-del	-/GAA	0.00119737	0.0244387	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1058229	CCTTTAAAACGCTGT[-/GAA]GAAGGTGCTTGCGGG	285498
rs563520389	snp	A/T	2.1193e-05	0.00325515	utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant	RNF212, LOC105374344	GRCh38.p7	4:1113505	GGCCGGGCCCACGCG[A/T]AGCCCACGCAAGGTT	285498
rs563523707	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1088109	GTTGGAACAATTTGG[A/G]GGGCTCAGAAAAAGA	285498
rs563537343	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1058727	GCAAGACCTGGAAAC[A/G]AACTGGCCAGTCCCA	285498
rs563602264	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1057623	GCAGCTGCCCCAAAA[A/G]CCAAACATATTTACT	285498
rs563660625	snp	G/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1082045	TGGTTGAGCCCAGGA[G/T]TTGGAGGCTACAGTG	285498
rs563675318	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1097400	ACAAGGTCAGGAGAT[C/T]GAGACCATCCTGTCT	285498
rs563774067	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1093203	TGCTCAGAGTTTTGG[C/T]CTTGGGCCAGTTTTG	285498
rs563854250	snp	C/T			downstream-variant-500B	RNF212	GRCh38.p7	4:1056062	AGTAATCACCTAACG[C/T]AGGATGTGGCGGCGC	285498
rs563876081	in-del	-/CAACACAGGGT	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1079236	GGACCAACATGGGAC[-/CAACACAGGGT]CAACACAGGACCAAC	285498
rs563899747	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1100010	CTCTGACTAGGAATG[C/T]CAGCCCTAATTTACT	285498
rs563960588	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1105038	GTTCTGCCTGCTGGG[A/G]TTCCCATCAAGTGAA	285498
rs563986026	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1089985	TACAGGGTGACAGGA[C/G]AGTGTAGGGGTGAGG	285498
rs563991470	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF212, TMED11P, LOC105374344	GRCh38.p7	4:1114883	TAGCAAGACCAGCAA[C/T]GTGGCAAAACCCCGT	285498
rs563999508	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1056793	CTTCTTTACACACGC[A/G]CTTTCCCAAGAGCAT	285498
rs564096590	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1105625	CATGAGACTGGAAAC[C/T]ATCAGAGGGTACTGC	285498
rs564100509	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1111907	CACCACACAACAATG[A/T]AAGTAGATGAACTAC	285498
rs564142204	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1099504	GGCTCCAGGAGCGGG[A/G]CGGGGAAGGCCAGGA	285498
rs564159871	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1111485	CCTGCTGGGTTCCCT[C/T]CCGCTGGGCTCCTCT	285498
rs564239945	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1106013	ATGGGGGACTTTGGC[A/G]CTTACTCCTGGAAAG	285498
rs564338053	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1080119	TACCACACCGTGCAC[A/G]CTCGGTACGCACTAG	285498
rs564356684	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1082068	CTACAGTGAGCTGTG[A/C]TTGTACTACTGTACT	285498
rs564490660	snp	C/G	0.0228947	0.104514	intron-variant	RNF212	GRCh38.p7	4:1095888	GCTCCATGGTCTCAG[C/G]ATAGCGCACCTGGCT	285498
rs564499853	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1108003	AACTTACTTTATGAA[C/T]AACACTCTTAATTAT	285498
rs564501605	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF212, LOC105374344	GRCh38.p7	4:1114674	ACGCCTGTAATCCCA[G/T]CTACTCCGGAGGCTG	285498
rs564563488	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	RNF212, LOC105374344	GRCh38.p7	4:1114204	CGCTGGCGCAGAGAC[C/T]TCAGCACGGGAGGCC	285498
rs564600869	snp	C/T	0.00199481	0.0315187	intron-variant	RNF212	GRCh38.p7	4:1067692	CAACATGGTGAACTC[C/T]GTCTCTACTAAAATT	285498
rs564635278	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1108659	CTTAAGGCTAAGTCT[A/G]TCCCAGGTATTTATT	285498
rs564828075	snp	A/G	0.00159617	0.0282053	intron-variant	RNF212	GRCh38.p7	4:1103020	ACTAACATTTGGCAC[A/G]CTGGTCAAGAGAAAA	285498
rs564883720	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1104067	TTGCATTTTTATATA[A/C]TAGCAATAAGCACTT	285498
rs564926521	in-del	-/ATATCCAGGAAATCACTGCCACATCCAACATTGTG	0.0023933	0.0345097	intron-variant	RNF212	GRCh38.p7	4:1066851	CTGTGCTTTGGTATC[lengthTooLong]ATATCCAGGAAATCA	285498
rs564931856	snp	A/C	0.000399281	0.0141238	downstream-variant-500B, intron-variant	RNF212	GRCh38.p7	4:1071055	TTTTTAAATACTGTT[A/C]TTACAATTTTTTCTG	285498
rs564935742	snp	C/T	1.66095e-05	0.00288175	missense, intron-variant, nc-transcript-variant	RNF212	GRCh38.p7	4:1081588	CTGAACTTTTTATTG[C/T]GCTGAAAGCTGTTTG	285498
rs564994165	snp	A/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1070673	AGTTACAGGTGGTTT[A/T]GTAGGACTGTGCTGT	285498
rs564994223	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1077185	GTGAGCCGAGATCTC[A/G]CCACTGCACTCCAGC	285498
rs565023610	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1098636	CAGGCATCAGGAGCT[C/T]AGAGTCTGGCCTAAA	285498
rs565062647	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1098040	ACTGCACTCCAGCCT[C/G]GGCAACAGAGCAAGA	285498
rs565069775	snp	C/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1065526	AGTCTGGGGTGCAGT[C/G]GTATGATCACTGCTC	285498
rs565079674	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1070631	GTTTTGTAGGACTGC[A/G]CTGTGTCAGCGTGGA	285498
rs565216390	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1059634	CCCTGGGGGTCTCTG[C/G]GGAACTATGAGTGGA	285498
rs565256039	snp	A/G	0.000399281	0.0141238	missense, utr-variant-3-prime, intron-variant, nc-transcript-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1073007	ACCTCAGCATATATT[A/G]GAAGTGTTTTAGAGT	285498
rs565291774	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1057652	CTACCTGCCCTTTAT[A/G]GAAGACGCCTGCTGA	285498
rs565304770	snp	C/T	0.00279162	0.0372561	intron-variant	RNF212	GRCh38.p7	4:1079032	AACACAGGACCAACA[C/T]GGGACCAACATAGAG	285498
rs565308225	snp	A/C	0.000399281	0.0141238	intron-variant, missense, downstream-variant-500B	RNF212	GRCh38.p7	4:1093669	GCAGCACTTGGCAAA[A/C]CCACCCTGGAGCGCA	285498
rs565318892	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1078373	CTGCCTCCTCTCTCC[C/T]GTTTCCGAGCTGCCT	285498
rs565328968	snp	C/G	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1111362	GTCTTGAGTTCCAGA[C/G]CCACATGTGCAACTG	285498
rs565381897	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1083005	CACAGTGAGGCCGGG[C/T]AAGACGGGGTCGGGG	285498
rs565441325	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1110158	GAGGAAATCACGTGC[A/G]GCCAAAAGACAAAGG	285498
rs565444874	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1073804	CAAGTTCCTGTCTAA[C/G]TTGATTCTGTGTTCA	285498
rs565571013	snp	A/G	0.00318978	0.0398085	intron-variant	RNF212	GRCh38.p7	4:1083756	AGGTGGCCTAAGACG[A/G]CGGAGATCACAGCAG	285498
rs565571605	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1104759	GTGGCCCCTTCCCTC[A/G]GGTCCCGATTTGGCC	285498
rs565576958	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1110533	GCAGAAACTATGTTA[A/T]GGTATGATAGCCAAA	285498
rs565584392	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1074307	CTGCCCCTTCCTGGG[C/T]TCGCTCCTCTGGCTC	285498
rs565634916	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1095595	TCCATGGTCTCAGCA[C/T]AGCGCACCTGGCTCA	285498
rs565636161	snp	A/T	0.00159617	0.0282053	intron-variant	RNF212	GRCh38.p7	4:1084173	TCAGGTTGGTCTCAA[A/T]CTCCCGACCTCAGGT	285498
rs565707286	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1091393	ATAAGGAGGAAAGAG[A/G]GTCCTGTGATTTCCT	285498
rs565723244	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1109951	CTCTTCTTCAAGTTG[C/T]CCTCATGCTAAAAAC	285498
rs565768690	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1111614	TTCTCCCCATCACCT[C/T]TCATGTGCTCAGCTG	285498
rs565770469	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1096003	ACAGCTCCATGGTCT[A/C]GGGATAGCGCACCTG	285498
rs565828012	snp	A/C	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1111048	AGCACCACGAAGGCA[A/C]ACGCGTCTCCATCAT	285498
rs565829036	snp	A/T	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1106388	GAAAATCCTGATAAT[A/T]AAAAAACCCACATAG	285498
rs565937582	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1057485	AACTGTGGTCTGTTC[C/T]GGGGCTGGGGCTGAG	285498
rs566006276	snp	C/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1111683	TTTCACCTCGCTGCC[C/G]GAGACACTTTTGTTT	285498
rs566018639	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime, intron-variant	RNF212, LOC105374344	GRCh38.p7	4:1113637	CCAACCTCGCGGGTT[C/T]TCCCGCAGCACCTGG	285498
rs566073121	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1057918	AATACAAAATTAGCC[A/G]AGTGTGGTGGCACAT	285498
rs566080086	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1113251	TCCTCCGCAGCCCCC[C/T]ACGTGCCCCCATGGC	285498
rs566173947	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1080135	CTCGGTACGCACTAG[C/T]TCCTTCATTTGCCAA	285498
rs566223480	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1066670	TTCGTTGTTAAGTTT[C/T]AGTTCTTTATGTATT	285498
rs566261395	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1074999	AACTACATTCCATTT[A/G]CTGCTCCATTTAGAG	285498
rs566293504	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1085763	TGCTCTGATGAAAGT[G/T]TCTGGTAAATGAACG	285498
rs566356060	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1089886	CCTTCCCAGTCATGC[A/G]GAACTGTGAGTCCAT	285498
rs566420497	snp	C/T	0.000165505	0.00909534	intron-variant	RNF212	GRCh38.p7	4:1090735	AGTCTGACATTTAAA[C/T]CTAAAGGTCAAAAAA	285498
rs566449335	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1061952	GGGCAGATGGCAGAG[A/G]CCCACGCTGTGCGGC	285498
rs566457520	snp	A/T			intron-variant	RNF212	GRCh38.p7	4:1068925	AGAAATCTATGAATA[A/T]GGCTGGACGCAATGG	285498
rs566544567	snp	C/G	0.0023933	0.0345097	downstream-variant-500B	RNF212	GRCh38.p7	4:1055795	GAACTAACCCCATAA[C/G]CCTCTTTTCCAACCC	285498
rs566553656	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1088577	AAATTCAAGCTGGCT[A/G]CAGAAATGTGCATAA	285498
rs566638519	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1082798	GGTGCTCAGTAAACA[C/T]TGGCTGCTGCGTGGC	285498
rs566672383	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1105873	GGAGGACATTCCAGT[C/G]AGAGGGGACAAGAAA	285498
rs566745750	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1109830	AGGCTTTCACTTGTG[C/T]ATCCATACTCGCCTC	285498
rs566781337	snp	A/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1078047	TGCCTTCTTATTCTG[A/T]CTCCGGGTCCCTCCA	285498
rs566794957	snp	A/G	0.00478085	0.0486577	intron-variant	RNF212	GRCh38.p7	4:1073742	CCACTGTCTGTTAGG[A/G]ACACATTTCCCAGAA	285498
rs566840951	snp	A/G	0.0193772	0.0965046	intron-variant	RNF212	GRCh38.p7	4:1066007	GTGTTCCAAGTAGCT[A/G]GGACTACAGGTGCGA	285498
rs566857053	snp	A/G	8.23649e-05	0.00641683	synonymous-codon, missense, intron-variant, nc-transcript-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1073063	ACTGAACGCTAGGAG[A/G]AGCAGCCAGTGAGGA	285498
rs566876706	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1066413	GACTTACTGCAACCT[C/T]TGCCCCCCAGGCTCA	285498
rs566885258	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1064879	TGACTACTTCACACA[A/C]ATGGACTCACACAGC	285498
rs566893013	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1104841	CCTGACATCTAATGG[C/T]GGCACGGGGCAGGAC	285498
rs566918413	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1078448	CAGGACAGACGACGG[A/G]AGAGCCGGGCCTGGA	285498
rs566982291	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1063129	TTAGATGGCAATACC[C/G]CCTACATTGATGTAC	285498
rs567024203	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1095123	TCCATGGTCTCAGGA[C/T]AGCGCACCTGGCTCA	285498
rs567041841	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1103656	ATTAAATGATAATCT[C/T]GACAGCTATAGAATA	285498
rs567043507	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1090217	CAAGACAGGGTGGGG[A/G]TGACAGGATGGAAGG	285498
rs567053939	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1061112	TCCCGTTGCAGCTTT[C/G]GGAGGAGCGGGACTT	285498
rs567084660	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1100226	CTAGCGTTAGGTCTT[C/G]TTTTGTGTTCCTGTC	285498
rs567150321	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1106696	AAGGTTAAGGGCTCA[C/T]CAGCCTCCAGCCCGA	285498
rs567156438	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1069521	GGTCAGGCGACCAAG[A/G]TGAACATCCTCCTGG	285498
rs567199154	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1075078	GCTGTCTGACAGCTG[C/T]GAGTTACAGAAGACA	285498
rs567208880	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1064279	GAGCAATGTGGTTAC[A/G]TTCCACTGGAATTCA	285498
rs567247929	in-del	-/A			utr-variant-3-prime, intron-variant	RNF212	GRCh38.p7	4:1071521	AAGGAAATGTCATCC[-/A]AAAAAAAAGACACAC	285498
rs567255987	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1113172	AGAGTTCCCCTGCTC[C/G]TCGCGGCCTCTCCCC	285498
rs567287612	snp	C/G	1.6507e-05	0.00287284	intron-variant	RNF212	GRCh38.p7	4:1081387	TCGGAAAGACCTGCA[C/G]GTCCTGTGATTTCTG	285498
rs567303598	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1092012	CCACCTTTGCCGACG[C/T]TTCTCAAGTCCTGCT	285498
rs567340825	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1091164	AATGGCCTCCTGACC[A/G]AACAGGTGTGGACCA	285498
rs567344807	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1102161	TTAAAGAACAAACTA[A/G]ATCCAGACAAAAAGG	285498
rs567393520	snp	G/T	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1107082	TTTTAGACTGAGTCT[G/T]GCTCTGTCGCCCAGG	285498
rs567423049	snp	A/G	0.00438332	0.0466095	intron-variant	RNF212	GRCh38.p7	4:1081742	CTGGGTTTGCAAACG[A/G]CATTTCACATGAATT	285498
rs567486559	snp	A/C	0.0107246	0.0724382	intron-variant	RNF212	GRCh38.p7	4:1102604	AAAAACAAAAAAAAA[A/C]CACTTTGGGAGGCTG	285498
rs567540612	snp	A/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1092631	GTGTTTATCTTGCAG[A/T]GAATATGCCTCTTGA	285498
rs567568804	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1076964	CAAAAATGTGTGCTG[A/G]CCAGGCTGTAATCCC	285498
rs567659388	snp	A/G/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1103149	TTTGAAAATTCCAAC[A/G/T]AAATGCACTAATTCC	285498
rs567677572	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1086398	AGGATCCCACTGTCC[A/T]GTCTGTAATCATGGC	285498
rs567680810	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1083311	TGGTGAAATGAGCAG[A/G]AATGTTCTCAAAATG	285498
rs567680992	snp	A/C	0.00159617	0.0282053	upstream-variant-2KB, intron-variant, utr-variant-5-prime	RNF212, LOC105374344	GRCh38.p7	4:1113792	GTGGCGGGCGCGGGG[A/C]ATGGCGGCTGCGCTG	285498
rs567827503	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1083692	CAGTGGGGTTCACTG[C/G]CTTAACCTGAAAATC	285498
rs567902613	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1105487	TGGTGACACACACTG[C/T]GAAGCAGAATAATCC	285498
rs567918964	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1059212	AGCCTCCGTGCCCCC[A/G]ACAGGGGTCTTGTCT	285498
rs567974690	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1064567	GCAGCCTTCTCACTC[C/T]GTCTTCATACGGCCT	285498
rs567990185	snp	C/G	0.00199481	0.0315187	intron-variant	RNF212	GRCh38.p7	4:1089596	AGGATATGAGATTTG[C/G]GAGGGGCCAGGGGTG	285498
rs567994924	snp	A/G	0.00676609	0.0577691	intron-variant	RNF212	GRCh38.p7	4:1100428	TTTTTTTTTTTTTGA[A/G]ATGGAGTCTTACCCT	285498
rs568095035	in-del	-/GAG	0.00119737	0.0244387	intron-variant, cds-indel	RNF212	GRCh38.p7	4:1094057	GCAAGGAAGCTCCCA[-/GAG]GAGGACAGTCTTGGG	285498
rs568133140	snp	C/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1100949	ATAGCTGTTCAGATG[C/G]AATTCTGCGGCTGAA	285498
rs568160570	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1065197	GTTTTTAAGTTTTGG[A/G]GGAAAGGCCACACTG	285498
rs568166495	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1110942	ACCTGTGAATCTATA[A/C]CTGCCCCAGGCCCTT	285498
rs568254233	snp	G/T			intron-variant	RNF212	GRCh38.p7	4:1064114	AATGATGGAATAAAA[G/T]ATTTTTTTCCTCTTA	285498
rs568279267	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1067148	ATTTAACTTTACCTC[C/G]TAAAGGTTCTAACTC	285498
rs568295496	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1067781	GCTGAGGCACAAGAA[C/T]TGCTTGAACCCAGGA	285498
rs568315579	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1095538	CATGGTCTCGGGATA[C/G]TGCACCTGGCTCATC	285498
rs568357718	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1074149	AGGCCGCTTCTGCCA[C/T]CATCCCTCCTCAACC	285498
rs568360123	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1082174	AAAAGAGAAAAGAAA[A/G]AAAAACAGGCCAGCA	285498
rs568449311	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1090901	GTGGCTGGAGTTTTG[C/T]TGGGGGAGGAGGAGG	285498
rs568513303	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1102912	TTTGGGAGGCCGAGG[C/T]GGGTGGATCACGAGG	285498
rs568546214	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1101126	GAGTTGGTGTGACCA[A/G]TATGAGCATTGGCAG	285498
rs568547926	in-del	-/ATAG	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	RNF212, TMED11P, LOC105374344	GRCh38.p7	4:1115069	AAAATAAGTTTAAGA[-/ATAG]GATGAGGTGCCTAAT	285498
rs568632293	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1085096	TGGGAGGCAGACAGG[A/G]CTCCTGACTCCTCGA	285498
rs568665940	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1091307	GACACCAGCACCCTC[C/T]CATTTACAGGAGCCC	285498
rs568673866	snp	A/G			intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1056511	ACTTCACACTGTTGA[A/G]GAAAATGAGGGTGCA	285498
rs568761413	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1111504	CTGGGCTCCTCTCCA[C/G]TGTTTTGTCTAGCAG	285498
rs568770710	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1080127	CGTGCACGCTCGGTA[C/T]GCACTAGTTCCTTCA	285498
rs568790264	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1089017	AGTGCAGAAGGGAAA[C/T]GTGCGGTGGTTGTTC	285498
rs568795496	snp	A/G	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1097622	AGCCCTCATGCAGAC[A/G]CTCCCAACTTCCTTC	285498
rs568826850	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1059750	AACCACAAATAATAA[C/T]GATGGCAGGTATCTT	285498
rs568826952	snp	G/T			intron-variant	RNF212	GRCh38.p7	4:1103966	ACATGTTGGCGTATG[G/T]AAATGTTCTAGCAGA	285498
rs568857435	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1098140	GACAAGATGTAGGAA[A/G]AACCTCATGCCTCCT	285498
rs568863821	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1064472	TGGGTGGCTTACACA[A/G]CAGAAGTTTATTTCT	285498
rs568959850	snp	A/G	0.00953873	0.0683987	intron-variant	RNF212	GRCh38.p7	4:1065970	CAGCCTTGACCTCCT[A/G]AGCTCAAGCAATCCT	285498
rs568964380	snp	C/T	0.00159617	0.0282053	intron-variant	RNF212	GRCh38.p7	4:1059203	GCACAAGGCAGCCTC[C/T]GTGCCCCCGACAGGG	285498
rs568966213	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1078074	TCCATCATCCGGCTC[C/T]GGGTGTGATTACCCA	285498
rs569099194	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant, intron-variant	RNF212, TMED11P, LOC105374344	GRCh38.p7	4:1115252	TATTTGTCCTTATTG[A/T]TAATATTTTAAACAA	285498
rs569108809	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1087949	AATTAAACCCCTTTC[C/T]TTTATAAATCACCCA	285498
rs569145804	in-del	-/C	0.00438332	0.0466095	intron-variant	RNF212	GRCh38.p7	4:1077386	AATCAATTTAGCCTG[-/C]CAGTCTTTTCTTTCT	285498
rs569163811	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1065470	TCCATTCTCCTCTCT[C/T]GTTTTCTTTTTTCTT	285498
rs569186340	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1082268	CGATGGCCAGTAGCA[C/G]AGACCACCTGCTGTG	285498
rs569210271	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF212	GRCh38.p7	4:1071610	CAATCCAATTAAAAA[A/G]TGGGCCAAATACCTT	285498
rs569234513	snp	C/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1060751	CTGTGTTCTGGAGGG[C/G]ACCGCGTACTGAAGA	285498
rs569267269	snp	C/T	0.00119737	0.0244387	utr-variant-3-prime, intron-variant	RNF212	GRCh38.p7	4:1072319	TTCCATATGCTGCTA[C/T]GATGGGGACACATGT	285498
rs569280385	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1109070	GGGAGTGTAATGACG[C/T]GATCTTGGCTCACTG	285498
rs569282406	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1084403	ACAATCTTCTAGAAA[C/T]GTAAAAGCCATGGTC	285498
rs569293694	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1109743	TCTAGACTGACCCAC[C/G]ACAGAACAACCCACT	285498
rs569311256	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1081150	TTGAGCGGGGGGCAC[A/G]CAGAACACTGGGTCA	285498
rs569407327	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1079590	TACTGAGGAAAATGG[A/G]AAATGCCACACGTCT	285498
rs569439848	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1094504	CTGAGAGGACTGGCA[C/T]AGCAGCTGGTAAAAG	285498
rs569488193	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1104805	AGAAAGACAATGAAC[A/G]TGTCTGCATCCTCGC	285498
rs569506234	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1069296	AAAGAAAAAGCTCTT[C/T]TTTATAGTAGAATGA	285498
rs569508470	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1062511	TCAACCCTATAAAGG[A/G]CGCCTCCAGGAAACC	285498
rs569564185	snp	A/C	0.00119737	0.0244387	downstream-variant-500B	RNF212	GRCh38.p7	4:1055925	ATGAGGAGGCTCCAC[A/C]CACGCAGGCCGCATC	285498
rs569616902	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1080065	CTGAGAGTGGGATCC[C/T]GAATTGACTTCTGTG	285498
rs569643707	snp	A/G	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1063095	CAACATTCATGGATT[A/G]GAAGATGCAGTGTTA	285498
rs569676612	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1111718	ATACACACCTGAAAT[C/T]AACAACTCCACTCCC	285498
rs569687395	snp	A/G	0.00159617	0.0282053	intron-variant	RNF212	GRCh38.p7	4:1085780	CTGGTAAATGAACGA[A/G]CTCTTCCCTCTGCAT	285498
rs569697468	snp	A/G			intron-variant, missense	RNF212	GRCh38.p7	4:1094256	GAAAGGAAGTGCAGG[A/G]CGGGGGCCAGGGGAA	285498
rs569713009	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1084979	TTCCCACAGGCCCCA[C/T]GGCCCCAGTGAGGCC	285498
rs569752636	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1092001	GGGCACCTTTCCCAC[A/C]TTTGCCGACGCTTCT	285498
rs569790140	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1102079	AAAATGAACACAGAA[A/G]GGAAGTTATGACCCT	285498
rs569858704	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1098840	GAGTGCGCAGGGAGC[A/G]GGAACTGTCACTGTT	285498
rs569871252	snp	A/C			missense, utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1072917	CAAAGAGGAAACACA[A/C]CAGACACAGCGGGTG	285498
rs569887173	snp	C/T	0.00199481	0.0315187	intron-variant	RNF212	GRCh38.p7	4:1107006	AAAATATAATGCAGT[C/T]CTTTTAAGAGTGAGT	285498
rs569932001	snp	C/T	0.00159617	0.0282053	intron-variant	RNF212	GRCh38.p7	4:1096623	GGCTCATCACAGAAC[C/T]AAGCACACCCCTCAC	285498
rs569992433	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1102708	ATACAAAAAATTAGC[C/T]GGGCGTGGTGGTGGG	285498
rs570055282	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1107643	TTTTAGTAGAGATGG[A/G]GTTTCACTGAGTTGG	285498
rs570224327	snp	A/C/T			intron-variant	RNF212	GRCh38.p7	4:1075184	GGGCTGTGTACGCAT[A/C/T]GGTGTGTTCACATCT	285498
rs570227692	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1058943	CCGGAAGGGCAAAAG[C/T]GCGTCCAGAATTTCT	285498
rs570236183	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime	RNF212, LOC105374344	GRCh38.p7	4:1113672	GCGCGTGTGACTCGT[C/G]TCCCAGGTCGTTTGG	285498
rs570240174	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1077330	CATTACATTCTGGTT[C/T]CTCAGCAATAATTTC	285498
rs570316989	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1070763	TTAGCGATGCTAGGG[C/T]ACCACATCGGTAACA	285498
rs570378105	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1070117	CTGTGTCAGCGTGGA[C/T]GCCTGGCCTGAGTTA	285498
rs570394252	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1104852	ATGGCGGCACGGGGC[A/G]GGACAGCTAAGAAAC	285498
rs570459087	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	RNF212	GRCh38.p7	4:1055908	CCCCACCCTCCTGAC[A/G]GATGAGGAGGCTCCA	285498
rs570459939	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1110335	AGACACCAAAGAGGA[A/G]AAAACAACAGGTGCT	285498
rs570502815	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1077990	GGCGTTTCTCTTTCA[C/T]GGAAGCTGTGACGGC	285498
rs570530888	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1105296	CTGCTCCGCGCTCAC[C/T]GGAGTCTCCCTTCCT	285498
rs570535420	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1082865	TCTGGCAGGGCCGTG[A/G]CCTGGCTCCTCTGAA	285498
rs570554584	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1101045	TTTCCAGATGCCAAA[C/G]ACTTGATTTTGATCT	285498
rs570600599	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1083173	CTCCCTCCAGCGAGA[C/G]TGGAAGAAAAGAAGG	285498
rs570662070	snp	A/G	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1083028	GGTCGGGGGCGCAGC[A/G]GTCTGGGGCGGGTCA	285498
rs570742029	snp	A/G	0.0182019	0.0936463	intron-variant	RNF212	GRCh38.p7	4:1078925	ACAGGACCAACACGG[A/G]ACCAACACAGGGTCA	285498
rs570777794	snp	A/G	1.64909e-05	0.00287144	missense, intron-variant, downstream-variant-500B, nc-transcript-variant	RNF212	GRCh38.p7	4:1073161	ACAAGGTCAACCATG[A/G]GATGAAACAGAAAGA	285498
rs570822988	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1057099	GTGGTTTTAAAGGCC[C/T]GGATTCAAAGGCATC	285498
rs570884634	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1061231	CACCTCCCCCTACCC[C/T]ACTCTACCCAGCAAG	285498
rs570917845	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1100814	TAGATGATTTCAGAC[A/G]AAAATGACCCATTAC	285498
rs571061609	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1095467	CTCCCACAGCTCCAC[G/T]GTCTCGGGATAGCGC	285498
rs571156336	snp	A/G	0.00279162	0.0372561	intron-variant	RNF212	GRCh38.p7	4:1075688	AACTCATAACCTTTT[A/G]TTTTTGAGACAAGGT	285498
rs571160942	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1102341	ACTAAAGTTCCACAG[C/T]TGGCCTTGTAGAACC	285498
rs571178946	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1102347	GTTCCACAGTTGGCC[G/T]TGTAGAACCTGCATA	285498
rs571246299	snp	C/T	0.00159617	0.0282053	intron-variant	RNF212	GRCh38.p7	4:1107536	TCTCACTGCAGGCTC[C/T]GCCTCCCGGGTTCAC	285498
rs571279103	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1058809	GAGCCTGCCCGTCAC[A/G]GGGGCAGCTGTGGGC	285498
rs571288271	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1077038	TTCGAGACCAGCCTG[A/T]CCAATATGGTGAAAC	285498
rs571348626	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1059129	GACTGTGACTGGCCA[A/G]TGCCCTGCCTGCTGC	285498
rs571396517	snp	A/C			utr-variant-3-prime, intron-variant	RNF212	GRCh38.p7	4:1072384	ACACCTAGAGTGAAC[A/C]CTAATGTAAACCATG	285498
rs571426595	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1077414	TCTTTTTTCTTTTTT[G/T]TAGAGACAGGGTCTC	285498
rs571439031	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1092960	CCTGTGCCTGCATTC[A/G]TCCACATGAGCTCCA	285498
rs571490324	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNF212	GRCh38.p7	4:1072159	AGTGAAAGGAGTCAA[C/T]CTGAGAAGCCACATA	285498
rs571525262	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1087870	ATGTGCCTTGCTCCC[C/G]CTTTGCCTTCTGCCA	285498
rs571602615	snp	A/G	0.000399281	0.0141238	intron-variant, missense, downstream-variant-500B	RNF212	GRCh38.p7	4:1093558	TCCACGGCCCATGCC[A/G]GAAGCCTGAGAGGCA	285498
rs571628536	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1065906	TTAAGAGACAGGATC[C/T]TACTCTGTCGTCCAG	285498
rs571660589	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1081774	AGCAGTTCCCATAGC[A/G]TCCTGTGAGTCGCAC	285498
rs571712636	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1104317	ATCTCAATGGCTTAT[A/T]GTGGGGACACTTGTT	285498
rs571741312	snp	C/G/T	0.000131963	0.00812203	synonymous-codon, utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1072970	CTCAGCCTGCTGGAA[C/G/T]GGAAACAAGACGGCC	285498
rs571753055	snp	G/T	0.00279162	0.0372561	intron-variant	RNF212	GRCh38.p7	4:1108916	ATGTTGCCCACACTG[G/T]GCTCGAACTCCTGGG	285498
rs571794664	snp	G/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	RNF212	GRCh38.p7	4:1099860	CTGTGCGGGATCCAC[G/T]GGGCTCTCCTCACGC	285498
rs571835933	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1103881	ACTGGAGGTCCCAGC[C/T]AATGCTGTAAAAAAA	285498
rs571867361	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1095241	TCCATGGTCTCGGGA[G/T]AGCGCACCTGGCTCA	285498
rs571893731	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1109692	ACTCAGAAGCAGCCC[C/T]GGCTCATGACCTACC	285498
rs571929631	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1059887	ATCACCTGAGGTCGG[C/G]AGTTCAAGACCAGCC	285498
rs571933053	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1100542	GCTCCCAAGTAATTG[A/G]GATTACAGGCGTGTG	285498
rs572054912	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1066658	TGAATCAGGTTGTTC[A/G]TTGTTAAGTTTTAGT	285498
rs572091709	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1105373	CTCTGCTCCCTGGCC[A/G]TCCACCACCCAACCA	285498
rs572179180	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1111885	GGGGTGTATCCATAC[A/G]ATGGAACACCACACA	285498
rs572188446	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1076120	CTTAGAAATTATCCC[A/G]CCAAGCCAGACACCT	285498
rs572193066	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1060977	TTATCTCTACGAAGC[A/C]AAGTGCGAAACTGGA	285498
rs572248189	snp	C/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1090513	GGCCCCAGTGTTGCC[C/G]CAGGTGGCTGAGGGG	285498
rs572248798	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1067221	TTTGGGGGGACTCAA[A/G]TCAGTCTATAGCAAA	285498
rs572255839	snp	C/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1056746	ACGTTTAGAGCTCCA[C/T]GGCTGCCCTTGGCAC	285498
rs572317170	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1112166	AAACCGAGATCCCGC[C/G]ACCGAACTCCAGCCT	285498
rs572389873	snp	C/G	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1091849	GGGTTCTCCCCTACT[C/G]GACAAGGGGACTATG	285498
rs572391428	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1111045	CCCAGCACCACGAAG[C/G]CACACGCGTCTCCAT	285498
rs572393740	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1057209	GCACCCAGGAGGGTC[A/G]ACAACCCAGGCCAGC	285498
rs572409285	in-del	-/A			intron-variant	RNF212	GRCh38.p7	4:1106362	CAATTACTGTGTATT[-/A]AAACCACAGTGAAAA	285498
rs572515369	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1065648	ATTTTTTGTAGAGAG[A/G]GGGTTTTGCCCAGGC	285498
rs572578419	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF212, LOC105374344	GRCh38.p7	4:1114603	CTTTCAAAAAATCCT[A/T]TTCAATGTGGAGACT	285498
rs572646865	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1075185	GGCTGTGTACGCATC[A/G]GTGTGTTCACATCTG	285498
rs572675416	in-del	-/G			frameshift-variant, intron-variant, downstream-variant-500B, nc-transcript-variant	RNF212	GRCh38.p7	4:1056882	TGCTGATGGGCGGCC[-/G]GGGGGGGCAGCCTGG	285498
rs572686399	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1101689	CTACTGAGTGTCATC[C/T]CTCCTCCAGCTCCTG	285498
rs572713428	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant, intron-variant	RNF212, TMED11P, LOC105374344	GRCh38.p7	4:1115387	GTATCTTCACTGGTC[A/G]TTCGAAAATTTTCTT	285498
rs572765786	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1093051	GCTGGGTGGATGGAA[C/T]GGATCTTAGAGGATT	285498
rs572784935	snp	A/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1068808	TTTTAAAATGTTAAT[A/T]TCATTGGATACAGAA	285498
rs572869186	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1070408	AGTTGTGGGTGGTTT[C/T]GTAGGACTGTGCTGT	285498
rs572869645	snp	A/T			intron-variant	RNF212	GRCh38.p7	4:1088915	GGAACCTCCACCTAG[A/T]TTTGAGAAGATGTAT	285498
rs572883110	in-del	-/G	0.00159617	0.0282053	intron-variant	RNF212	GRCh38.p7	4:1084539	GTCCAAGACTAGCCT[-/G]GGTAACATAGTGAGA	285498
rs572883552	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1060062	TGAGATCACACCATT[A/G]CACTCCAGCCTGGGC	285498
rs572958984	snp	C/T	0.000798403	0.0199641	downstream-variant-500B	RNF212	GRCh38.p7	4:1055982	CATCTCTGGACCTGA[C/T]GGAGATTCACCCGCT	285498
rs572966455	snp	G/T	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1081907	CTGCGGGTGTTAAAG[G/T]TGTGAAATTAAGACC	285498
rs573019718	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1060406	CTCGGAGAAAGGGGC[C/T]GCCAGGGATGCTAGA	285498
rs573038907	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1104034	TGCAAGGTCACTAGA[A/G]ACAGTTAAGAAAATC	285498
rs573099589	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1064825	CCTCCATCCCACAGC[C/T]GCTGGCAGCCACCAT	285498
rs573102403	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1109247	TCCTGACCTCAGGTG[A/G]TCAGCCCACATCGGT	285498
rs573136710	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1083735	GAAGCAACCCAGCAT[A/G]TGACCAGGTGGCCTA	285498
rs573194444	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1078318	AAGTCCTGATCCCTC[C/T]TATGGGGTGCAGCTC	285498
rs573198023	snp	G/T			intron-variant	RNF212	GRCh38.p7	4:1057115	GGATTCAAAGGCATC[G/T]CTGAGAACCTCGGAG	285498
rs573283016	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1088819	TTGGGCTGCTGCTTC[A/G]GAGGGAGCAAACCCC	285498
rs573353761	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1094017	AAAGCCTGAGATACT[A/G]TGGGTGATTCAGGCT	285498
rs573362337	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1058086	AAAAGCAAACTCTAA[A/G]GTGGTATATACAACA	285498
rs573406492	snp	A/G/T			intron-variant	RNF212	GRCh38.p7	4:1101775	CTCTTCCTTCTCAGC[A/G/T]CAAAAATATCTGTAC	285498
rs573444512	snp	C/T	0.00166806	0.0288313	intron-variant, utr-variant-5-prime	RNF212	GRCh38.p7	4:1099773	AGAGGGCGTAAGGAA[C/T]GGAGGAAATCAACCC	285498
rs573475137	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1083365	AACTCAATGGGGGCC[A/G]GGTGTGGTGGCTCAC	285498
rs573589394	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1080410	AACAGTTTCCAGTTC[G/T]CCACCCGCTCCCAGT	285498
rs573628963	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1068196	TTAGAGGGCTATGCC[A/G]TCTAATTCCAAAACT	285498
rs573671438	snp	A/G	0.00199481	0.0315187	intron-variant	RNF212	GRCh38.p7	4:1076018	GTATTTGTGAGTCAT[A/G]ATTTTACCTTTTCAA	285498
rs573697575	snp	G/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1095769	AGCTCCATGGTCTCA[G/T]CATAGCGCACCTGGC	285498
rs573735211	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1085401	TAAGTCCCCATTTTG[A/G]TTAATCCTAGCAACT	285498
rs573759162	snp	A/C	0.00199481	0.0315187	intron-variant	RNF212	GRCh38.p7	4:1096290	CACCCCCCACAGCTC[A/C]ACGGTCTCGGGATAG	285498
rs573763413	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1102441	GCATCTGACTGGAAA[A/G]ATCTCTATGTATACA	285498
rs573798624	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1091650	CCCGGTGCAAACACA[A/G]GGCAGGCTTCTTCCC	285498
rs573827911	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1112297	TGGTTGTAGGGCTGC[A/T]TTCACTAAGGCTCCA	285498
rs573845600	snp	A/G	3.33673e-05	0.00408442	intron-variant	RNF212	GRCh38.p7	4:1085846	AGACGACCAATGCAC[A/G]TGGCAGTGGGTGCCT	285498
rs573899713	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1102759	CGGGAGGCTGAGGCA[C/G]GGGAATGGCGTGAAC	285498
rs573899951	snp	A/C/G	3.29762e-05	0.00406045	intron-variant	RNF212	GRCh38.p7	4:1096885	TTGTGTCTAATAAAC[A/C/G]CTTCTGGCCCCCAGT	285498
rs573984829	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1075309	ATAAATACCAGAGAC[C/T]GTGTAATTCATAAAG	285498
rs573990798	snp	C/T	1.7612e-05	0.00296744	missense, upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant	RNF212, LOC105374344	GRCh38.p7	4:1113385	GCGTCGCAGTACACG[C/T]GCCCGCAGTTGGTGA	285498
rs574134700	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1065771	TTGGCATTTTTAGTA[A/G]AAACAGGTTTCATCA	285498
rs574159822	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1104696	CCCCCAGAGTGGAGC[A/G]CCCCCACCACCACTG	285498
rs574272447	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1058621	TCTTCCACATGAGGG[C/T]GTAAATATCCTACAT	285498
rs574297631	snp	A/G	0.00159617	0.0282053	intron-variant	RNF212	GRCh38.p7	4:1099323	GCACTAAAATAAATA[A/G]TAAAGGAATTCCCTG	285498
rs574341798	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1104032	TCTGCAAGGTCACTA[C/G]AGACAGTTAAGAAAA	285498
rs574409910	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1058946	GAAGGGCAAAAGCGC[A/G]TCCAGAATTTCTTTC	285498
rs574429035	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	RNF212	GRCh38.p7	4:1099822	TCCACAAGGTCCGAC[A/G]GCGCAAGCGGACACG	285498
rs574604591	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1056607	TTCAGATGTCATCTT[A/G]GTATTTTCAGAGTAT	285498
rs574614728	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1062655	AGTTCCAGAGAGGGC[A/G]GTTAGGCGAGAAAAA	285498
rs574625160	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1094830	GAGGGGGCATCTTGC[A/G]CAAAGGACCCCAGAA	285498
rs574669152	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1060512	GGGTGCCAAGGGGGC[A/G]CCATGTTTCAGTCCC	285498
rs574767554	snp	G/T	0	0	intron-variant	RNF212	GRCh38.p7	4:1057165	CGGCGGCCAGCAGAA[G/T]ATGTGGACCGATGCT	285498
rs574797799	snp	A/G	0.0349115	0.127424	intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1112184	CGAACTCCAGCCTGG[A/G]CGACAAAGCTGAGCT	285498
rs574811137	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1078323	CTGATCCCTCCTATG[A/G]GGTGCAGCTCACTCT	285498
rs574817025	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1070064	TGCTGTCAGCGTGGA[C/T]GCCTGGCCTGAGTTA	285498
rs574838478	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1083552	CTGAGGCAAGACAAT[C/T]GCTTGAACCCGGCAG	285498
rs574897169	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1086272	GTCACACACAAGCAC[A/C]TTCCATACACGGCCA	285498
rs574908728	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1073899	ATTCCCTCTGTTCCA[C/T]CAGGGCCTAAAACAG	285498
rs574923029	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1111327	CCCGTATTAATCGCT[C/T]CCCAAATGTGTTCCT	285498
rs575041744	snp	A/G	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1105818	TCCTCACATTCCATA[A/G]AGACTTAAGGCTGTG	285498
rs575050820	snp	C/T	3.30879e-05	0.00406729	intron-variant	RNF212	GRCh38.p7	4:1079601	ATGGGAAATGCCACA[C/T]GTCTGGTATACAGAG	285498
rs575063983	in-del	-/TT	0.332799	0.23589	intron-variant	RNF212	GRCh38.p7	4:1100399	AGGCATTTTCCATAA[-/TT]TTTTTTTTTTTTTTT	285498
rs575082130	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1092765	GCTGCCCGGTGCTCA[C/T]GCGTGCTTTGCCCGC	285498
rs575210244	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1092185	GAACCTACCAGCAGA[C/T]GCGCCTCATCCCGGC	285498
rs575239623	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1105520	GTCAAGGAACACAGC[A/G]TCAGAGGGTCACTTT	285498
rs575287249	snp	C/T	0.00358779	0.0422022	intron-variant	RNF212	GRCh38.p7	4:1060010	GAGGCAGGAGAATCA[C/T]TTGAACCTGGGAGGC	285498
rs575371055	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1076649	GTGGGGCAGGGAGGA[C/T]GGGAGCTCTTTCCAA	285498
rs575385505	snp	C/G/T	0.011919	0.0763696	upstream-variant-2KB, intron-variant	RNF212, LOC105374344	GRCh38.p7	4:1114090	TGTGGGGGCGTGAGG[C/G/T]GGTGGGGGTGGGGTG	285498
rs575386497	snp	C/G	0.0023933	0.0345097	intron-variant	RNF212	GRCh38.p7	4:1088792	CATGACTAAAAGGGT[C/G]CAAGGTACAATTTGG	285498
rs575400148	snp	A/G	0.00914312	0.0669923	intron-variant	RNF212	GRCh38.p7	4:1086773	GGCATAGGGGTGGAA[A/G]GACAGGGGTGGGGTG	285498
rs575411099	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1099536	AAGGGGGATCGGTGA[A/G]AGCTGAGGCCCTCGC	285498
rs575447014	in-del	-/T			intron-variant	RNF212	GRCh38.p7	4:1066820	GGTCAATTTGTTTAA[-/T]TTTTTTTTTTTGTTG	285498
rs575520730	snp	C/T	0.00478085	0.0486577	intron-variant	RNF212	GRCh38.p7	4:1089213	ACAGAGCCACAGGGG[C/T]GGAGTTGCCCAAGGC	285498
rs575522671	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1082573	ACCACTGGGGCCTCC[A/G]CTCTGAGTCACCTCC	285498
rs575534808	snp	A/C/G	3.30258e-05	0.0040635	intron-variant	RNF212	GRCh38.p7	4:1081500	AAAATGCCAGCGTCA[A/C/G]TGCACACAGTGTGAC	285498
rs575588302	snp	A/G	0.00318978	0.0398085	intron-variant	RNF212	GRCh38.p7	4:1070956	TTATTTTAAAAAACT[A/G]ATTTGTTTTTTTAAA	285498
rs575609121	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1067370	AAATTAATAATTATA[C/T]AAAATATCAATGGAC	285498
rs575672534	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1073836	CTCCCGACTCTGCCT[G/T]CTGGTGGTAGAGGTG	285498
rs575749222	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1068048	GCAATTCTCCCCACA[C/G]CGATGTAGAGATTCA	285498
rs575762245	snp	C/T	0.000399281	0.0141238	intron-variant, missense, downstream-variant-500B	RNF212	GRCh38.p7	4:1093594	GGCAGAGCAGACAGG[C/T]GGCTGGAGGGGCTGG	285498
rs575837648	in-del	-/TT	0.325799	0.238232	intron-variant	RNF212	GRCh38.p7	4:1083946	TCCACATTTTGTGCA[-/TT]TTTTTTTTTTTTTTT	285498
rs575845941	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1090529	CAGGTGGCTGAGGGG[A/G]TAAGTGTGGCCAGGC	285498
rs575847348	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF212, TMED11P, LOC105374344	GRCh38.p7	4:1115485	GGGTTGTTGTGGGCA[C/T]TCAAGGTATTTAATA	285498
rs575850537	snp	A/G/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1103904	TAAAAAAAAGGAAGC[A/G/T]CATAAGGAATAGAAA	285498
rs575929113	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1091536	ACTGGTACTGAAAGT[C/T]GGCGTCCTCTAGCTC	285498
rs576011266	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1057243	GACGGGAGGTGGGGG[C/T]GTGAGAGAACGCTGA	285498
rs576020008	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1111917	CAATGAAAGTAGATG[A/G]ACTACAGTTACATAC	285498
rs576033106	snp	C/G	0.021333	0.101051	intron-variant	RNF212	GRCh38.p7	4:1095357	GCTCCATGGTCTCAG[C/G]ATAGCGCACCTGGCT	285498
rs576065067	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1085302	AGAACAGATGCAATA[C/T]GGCAAAAGCACGGAT	285498
rs576179824	snp	G/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1057570	CATTAATTTACACAC[G/T]GCCTGCCCCGGCCTT	285498
rs576208482	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1095635	CAAGCACACCCCCCA[A/C]AGCTCCATGGTCTCG	285498
rs576249792	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1105752	AAAGCGTCCTTCCAC[C/G]GCAGGTCAGGGTCAA	285498
rs576307239	snp	A/G	0.00438332	0.0466095	downstream-variant-500B, intron-variant	RNF212	GRCh38.p7	4:1070996	TACAATTTTTTCTGT[A/G]TGCTTGAAGTATTTT	285498
rs576359289	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1080211	TCCTAGCCCTGCCAT[A/C]CTTATGGCTCGTGAT	285498
rs576370134	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1102406	GGTTTTGTATCTCAT[G/T]AATACTGTATTTTTG	285498
rs576371304	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1096573	CAGAACCAAGCACAA[C/T]TCCCACAGCTCCATG	285498
rs576422843	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF212, LOC105374344	GRCh38.p7	4:1114681	TAATCCCAGCTACTC[C/T]GGAGGCTGAGGCAGG	285498
rs576463134	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1088687	CCCAGAGAAAAAAAG[C/T]AGTTTTATGGGCCGG	285498
rs576509556	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1112174	ATCCCGCCACCGAAC[A/T]CCAGCCTGGGCGACA	285498
rs576599140	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1076009	ATTCATTTTGTATTT[G/T]TGAGTCATGATTTTA	285498
rs576627275	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1058548	CACACAGGCACGCGG[A/G]GTCCTCTTAGGTTGC	285498
rs576688286	snp	A/G	0.00438332	0.0466095	intron-variant	RNF212	GRCh38.p7	4:1069554	GAATCAGGCGACCAA[A/G]GTGAACATCCTCCTG	285498
rs576688294	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1062716	TGAAAAGATAAAAAT[A/G]AAAGTAAAAGATAAA	285498
rs576735061	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1082497	GATACGAACAGTCTG[C/T]CCTCAGCAGTTTCAG	285498
rs576827003	snp	A/T			intron-variant	RNF212	GRCh38.p7	4:1075924	TGACTCAGCTCCCAA[A/T]GTGTTAGGATTACAG	285498
rs576893634	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1078738	ATGGGACCAGCAGAG[A/G]ATCAACGCAGGATCA	285498
rs576977115	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1104101	AAAAATTGTTTAAAA[C/T]TACAATAGTAGCAGT	285498
rs577020025	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1060467	CAGCTCTCGAGAGCA[C/T]CGCAGCCCTGAGGTG	285498
rs577049436	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1104293	ACTGGTGTATCAGAC[A/C]ACCCCCAAATCTCAA	285498
rs577097487	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1110084	TAAAAGATTAACAGA[C/G]CCGACTCATAAAAAT	285498
rs577102100	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1062263	ACAAAATCCAGCAGC[A/G]TATAAGAAAGATCAT	285498
rs577159968	snp	C/T	0.00159617	0.0282053	intron-variant, missense	RNF212	GRCh38.p7	4:1094257	AAAGGAAGTGCAGGG[C/T]GGGGGCCAGGGGAAG	285498
rs577174761	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1081259	GGGACCTGAGCCTCG[C/G]AGGGAGATGAAATAA	285498
rs577217038	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1099034	TGTCCAGAAGATGAG[A/C]CTAGAGCCAGAACAG	285498
rs577230809	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1094620	ACAGCAGGGGCTCAG[A/C]TGCCAGAAGGGGGGC	285498
rs577253549	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1097676	CCTCACCTCCCTGCA[C/T]CTCTGGCCTTCCCTC	285498
rs577267096	snp	G/T	0.00318978	0.0398085	intron-variant	RNF212	GRCh38.p7	4:1083014	GCCGGGCAAGACGGG[G/T]TCGGGGGCGCAGCGG	285498
rs577271732	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1089323	GCTGCCCTGCTGGGT[C/T]CTGGACTTGCATGGG	285498
rs577331409	snp	G/T	0.00119737	0.0244387	intron-variant	RNF212	GRCh38.p7	4:1078749	AGAGGATCAACGCAG[G/T]ATCAACACAGAACCA	285498
rs577400324	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1083499	AATACAAAAATCAGC[C/T]AGGCGTGGTGGGGCT	285498
rs577413167	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1089726	GGGGGCAGTTTCCCC[C/T]GTGCTGTTCTCGTGA	285498
rs577476850	in-del	-/CGA	0.00478085	0.0486577	intron-variant	RNF212	GRCh38.p7	4:1101263	AGTTATATCCTTCTG[-/CGA]GTCTTTTGTCCCTTT	285498
rs577519557	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1076033	GATTTTACCTTTTCA[A/G]AAAGATATGTTAATC	285498
rs577642138	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1110576	CAACCTTAAGAATGA[C/T]GATACAGACTTATTT	285498
rs577655502	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1069906	TCTTGACCAGAGGAG[A/G]AGAAAAACTCTGTGG	285498
rs577660733	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1085554	TGCAGGTGGAGTCCC[A/G]CAGTCCCTGGCTGCA	285498
rs577665956	snp	C/T	0.233235	0.249437	intron-variant	RNF212	GRCh38.p7	4:1096469	CCCCCCACAGCTCCA[C/T]GGTCTCGGGATAGCG	285498
rs577738155	snp	A/C	0.000798403	0.0199641	intron-variant	RNF212	GRCh38.p7	4:1080868	CCCAGGCCGGGTTTT[A/C]TCTGGGATGCTGGAG	285498
rs577776546	snp	G/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1093144	AGTGGCTGAGGTGGT[G/T]TGTTGACGCTGTCCC	285498
rs577806226	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1110843	ATTTGGTGTGGTCCC[A/G]ACATGCAGCATCTGT	285498
rs577811180	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1108664	GGCTAAGTCTATCCC[A/G]GGTATTTATTACAAT	285498
rs577840513	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1092812	GGCCGCGAAGGCCTG[A/G]GAGTCAAGGCAGTCG	285498
rs577854995	in-del	-/AAAT	0.00478085	0.0486577	intron-variant	RNF212	GRCh38.p7	4:1083663	AACAAACAAACAAAC[-/AAAT]AAACAAACAAACTCA	285498
rs577914579	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1088041	GAGTGGGGCACTGCT[A/G]TAAATGTAACTAAAA	285498
rs577978624	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1107316	TCAGCCTCCCAAAGT[G/T]CTGGGATTACAGGTG	285498
rs578020474	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1103248	AAAGATATCAAATCC[C/T]TAGTTTAAAATCTTT	285498
rs578059835	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1064162	AAGTTTAATTCAGGA[A/G]ATAATGACAACACCA	285498
rs578081429	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1102809	GTGAGCCAAGACTGC[A/G]CCACTGCACTCCAGC	285498
rs578103637	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212	GRCh38.p7	4:1059340	GCTAAGAGCAAGAAG[G/T]AAAGCTGTCTTACTA	285498
rs578219002	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1067518	AAAGATATACCATGT[A/G]AACTATAACCAATAT	285498
rs578241064	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1090357	CCAGACTTGGGGAAG[C/T]GGCCCCAGGTTCCCT	285498
rs578246791	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1089737	CCCCCGTGCTGTTCT[C/T]GTGATAGTAAGTTCT	285498
rs745339926	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1100848	AATCATCAGGTTCTT[C/T]AGTGTAGATGCCTAT	285498
rs745356767	in-del	-/CAACCCACA	1.64992e-05	0.00287216	intron-variant	RNF212	GRCh38.p7	4:1081407	TGTGATTTCTGCAAG[-/CAACCCACA]CACCTGTCGGGGGCT	285498
rs745375972	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1063241	ATGCAAGGAACTCAA[A/C]ATATGCAAAACAATC	285498
rs745419157	snp	A/G	1.65792e-05	0.00287912	missense, upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant	RNF212, LOC105374344	GRCh38.p7	4:1113424	CACGACGTCCTGTGG[A/G]GCGGCTGGAAGCAGC	285498
rs745428146	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1099989	CCGCTAGGCAGGAAC[A/G]GGGTTCTCTGACTAG	285498
rs745464388	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1073795	GCCCTCTGACAAGTT[C/G]CTGTCTAACTTGATT	285498
rs745467340	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1102627	GGAGGCTGAGGCAGG[A/C]AGATCACGAGGTCAG	285498
rs745543953	in-del	-/AAG			intron-variant	RNF212	GRCh38.p7	4:1060111	CAAAAAAAAAAAAAA[-/AAG]AAGAAAAAAGAAATT	285498
rs745562832	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1083507	AATCAGCCAGGCGTG[A/G]TGGGGCTGTAATCCC	285498
rs745632018	in-del	-/T			intron-variant	RNF212	GRCh38.p7	4:1105300	CCGCGCTCACCGGAG[-/T]TCTCCCTTCCTGGCG	285498
rs745743790	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1105704	CTCACACACGGATGC[A/G]CCCACGTGCAAGTGC	285498
rs745790768	snp	A/G	1.6495e-05	0.0028718	missense, intron-variant, nc-transcript-variant	RNF212	GRCh38.p7	4:1081440	GGGGCTGATGAGTGA[A/G]GTGGCAGCAGGCATC	285498
rs745791872	snp	G/T			intron-variant	RNF212	GRCh38.p7	4:1065316	TGGGTTTTTAAAAAT[G/T]ATTACAATAAACATT	285498
rs745837976	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1089928	CCTTTATAAATTACC[A/G]AATCTCAGGTTATTC	285498
rs745858799	snp	A/G	1.6477e-05	0.00287024	intron-variant	RNF212	GRCh38.p7	4:1096847	GCGTCGGTCTGAAAG[A/G]GAAAGAAATGACTCT	285498
rs745908554	snp	G/T			missense, upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant	RNF212, LOC105374344	GRCh38.p7	4:1113420	GAAGCACGACGTCCT[G/T]TGGGGCGGCTGGAAG	285498
rs745938589	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1065070	ATGGCTCCCATGTTT[C/T]AGACACTGTGAATAA	285498
rs745959710	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1077788	AGCTTCCAGCAGGGC[C/T]TGAGGGGGCAGGTGG	285498
rs745967759	snp	C/T	4.95814e-05	0.00497878	intron-variant	RNF212	GRCh38.p7	4:1081517	GCACACAGTGTGACT[C/T]AGCAACATGCATCTC	285498
rs746023255	snp	A/G			upstream-variant-2KB, intron-variant	RNF212, TMED11P, LOC105374344	GRCh38.p7	4:1115094	GTGCCTAATCTATCA[A/G]ATTCAGAAGCTGCAT	285498
rs746145696	snp	A/G	4.19437e-05	0.00457931	utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant	RNF212, LOC105374344	GRCh38.p7	4:1113504	AGGCCGGGCCCACGC[A/G]AAGCCCACGCAAGGT	285498
rs746179974	snp	C/T	1.6492e-05	0.00287154	missense, utr-variant-3-prime, nc-transcript-variant	RNF212	GRCh38.p7	4:1073622	CCATCTTGAGGTGGA[C/T]TAATCATGGAGATTC	285498
rs746215556	in-del	-/CTAACGCAGGAT			downstream-variant-500B	RNF212	GRCh38.p7	4:1056056	ATGCGTAGTAATCAC[-/CTAACGCAGGAT]GTGGCGGCGCCGACC	285498
rs746314383	snp	G/T			intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1093222	GGGCCAGTTTTGCAC[G/T]CTTAAAAGTTACTGA	285498
rs746322715	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1111381	CATGTGCAACTGCCT[A/C]TTGTCTTCCCCTGGA	285498
rs746338069	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1057476	GGGGAGGTGAACTGT[A/G]GTCTGTTCCGGGGCT	285498
rs746404434	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1092231	TCTGGCTGTTCTTAG[A/G]GAAAGGCCTTGGGGA	285498
rs746460092	snp	A/G	1.68371e-05	0.00290143	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1073213	GGGAAGATGCAGGAG[A/G]CAGCGTGTGGGGAGA	285498
rs746503250	in-del	-/T	0.000616143	0.0175411	intron-variant, utr-variant-3-prime	RNF212	GRCh38.p7	4:1094053	GAAGCAAGGAAGCTC[-/T]CCAGAGGAGGACAGT	285498
rs746523433	snp	C/T	1.64749e-05	0.00287005	synonymous-codon, missense, intron-variant, downstream-variant-500B, nc-transcript-variant	RNF212	GRCh38.p7	4:1073132	GACACACTCTCCGGG[C/T]ACAGGGGGCTTAGAC	285498
rs746551060	snp	C/G	1.65625e-05	0.00287766	intron-variant	RNF212	GRCh38.p7	4:1090854	CTGAAAAGATCATAG[C/G]TTTCAGCTGCTGACA	285498
rs746580998	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1102260	TAGTTTTTGAAAATA[C/T]AGTCATCCTTCAGTA	285498
rs746599446	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1090022	AGGATGGGATGAGGG[C/G]TGACGGGATGGGATG	285498
rs746673442	snp	A/G			intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1073586	GTCTGAGGTTACAGG[A/G]CATTTTACTTACCCA	285498
rs746700611	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1075265	AGTTTTCACATTTAA[A/C]TGGTGTATTAGGCCA	285498
rs746702751	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1063438	GGAAATGGCTGGGTA[C/T]GGTGGCTCATGCCTG	285498
rs746744686	snp	A/G	1.65293e-05	0.00287479	intron-variant	RNF212	GRCh38.p7	4:1081528	GACTCAGCAACATGC[A/G]TCTCTATTTTGTTCT	285498
rs746772873	snp	C/T			utr-variant-3-prime, intron-variant	RNF212	GRCh38.p7	4:1071879	TCTTTCAAAACTAAA[C/T]ACCCTCTCACCATCT	285498
rs746846634	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1096264	CACCTGGCTCATCAC[A/G]GAACCAAGCACACCC	285498
rs746878154	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1097684	CCCTGCACCTCTGGC[C/T]TTCCCTCACTTTCCC	285498
rs746904667	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1070014	TGTGTCAGCGTGGAC[A/G]CCTGGCCTGAGTTAC	285498
rs746928228	snp	A/C/G			intron-variant	RNF212	GRCh38.p7	4:1085342	TGTACAAGAAAGGAG[A/C/G]GTTTCAAATGGCTAG	285498
rs746936890	snp	C/T	3.40205e-05	0.00412421	intron-variant	RNF212	GRCh38.p7	4:1081625	TGATCTCATACTAAA[C/T]AGATGGAGAAAAGGT	285498
rs746953562	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1106607	TGCACAGAAAGACAC[A/G]GATGGTCTTAAATAT	285498
rs747050608	snp	C/T			intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1058017	GGTGAGCCAAGATGG[C/T]GCTACTGCACTCCAG	285498
rs747107572	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1067948	GTGAAAATTGCTGAG[A/G]ATTCTTGAGAGAAAC	285498
rs747116297	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1080932	ATGGCCAGGCAGGCA[C/T]AGCCTGGAGATGGGG	285498
rs747133368	snp	C/T	3.30344e-05	0.004064	synonymous-codon, utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1072875	CACATAAATGCAAAT[C/T]AAAATGACTTTTTCC	285498
rs747260404	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1089068	GGTGCTGCCTAGAGA[A/G]GCCATGAGAAGAGGG	285498
rs747260983	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1078479	CTCTCCCTGAGTTCC[A/G]GGCAGGTTTCCTCTG	285498
rs747355265	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1091851	GTTCTCCCCTACTCG[A/G]CAAGGGGACTATGTC	285498
rs747375561	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1111314	ATAGGATTATTATCC[C/T]GTATTAATCGCTCCC	285498
rs747396076	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1110354	ACAACAGGTGCTCAC[A/G]TGTCACTACAGGGAA	285498
rs747404537	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1083705	TGGCTTAACCTGAAA[A/G]TCAGGGAGCTGGAAG	285498
rs747506534	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1094626	GGGGCTCAGCTGCCA[A/G]AAGGGGGGCCCACGG	285498
rs747565743	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1108120	TCCAGGAACACAGCA[C/T]GATTCAACAACCTAG	285498
rs747585589	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1083022	AGACGGGGTCGGGGG[C/T]GCAGCGGTCTGGGGC	285498
rs747700354	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1091966	ACCCCAGCTCTTGTG[C/T]ACATTGCAGGCCATG	285498
rs747706799	snp	A/G	1.64925e-05	0.00287158	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	RNF212	GRCh38.p7	4:1073609	CTTACCCATTCGTCC[A/G]TCTTGAGGTGGACTA	285498
rs747755109	snp	C/G			intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1056608	TCAGATGTCATCTTA[C/G]TATTTTCAGAGTATT	285498
rs747756360	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1069625	GACTAAGGTGAACAT[A/C]CCTGTGGCAGAACAG	285498
rs747767304	snp	A/G	1.65496e-05	0.00287655	missense, utr-variant-5-prime, intron-variant, nc-transcript-variant	RNF212	GRCh38.p7	4:1108362	TTTGAAAGCAAAACT[A/G]TACGACAAGGAGCTT	285498
rs747829066	snp	A/G	2.09905e-05	0.00323957	missense, utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1072905	CTTTCAAATTGGCAA[A/G]GAGGAAACACAACAG	285498
rs747843039	snp	A/G			downstream-variant-500B	RNF212	GRCh38.p7	4:1055830	TGGTCCCGGCTGGCG[A/G]GAGAGACCTGGGCTC	285498
rs747881207	snp	G/T			intron-variant	RNF212	GRCh38.p7	4:1064932	TATGCACTTAGCATA[G/T]CGTCCTCAATGTTCA	285498
rs747898462	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1061957	GATGGCAGAGGCCCA[C/T]GCTGTGCGGCCCAGA	285498
rs747901402	snp	A/G			upstream-variant-2KB, nc-transcript-variant, intron-variant	RNF212, TMED11P, LOC105374344	GRCh38.p7	4:1115251	TTATTTGTCCTTATT[A/G]ATAATATTTTAAACA	285498
rs747914881	snp	A/G	1.71941e-05	0.00293202	intron-variant	RNF212	GRCh38.p7	4:1081631	CATACTAAATAGATG[A/G]AGAAAAGGTATTGAA	285498
rs747946336	snp	A/T			intron-variant	RNF212	GRCh38.p7	4:1083041	GCGGTCTGGGGCGGG[A/T]CAGCTGGGCTGGCAG	285498
rs748065928	snp	G/T			intron-variant	RNF212	GRCh38.p7	4:1100164	GCCTGTGTGGACTTT[G/T]CACGGTTTCAGAATC	285498
rs748124857	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1109263	TCAGCCCACATCGGT[C/G]TCTCAAAGTGCTGGG	285498
rs748136638	snp	C/G			utr-variant-3-prime, intron-variant	RNF212	GRCh38.p7	4:1072043	AGTAGGTGAATGGAT[C/G]AACTATGATACATCC	285498
rs748166312	snp	A/C/G	3.3093e-05	0.00406763	intron-variant	RNF212	GRCh38.p7	4:1079620	TGGTATACAGAGGAA[A/C/G]TCAGCAGGAGAGATG	285498
rs748210235	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1097461	TATAAAAAAATTAGC[A/C]GGGCGTGGTGACGGG	285498
rs748256510	snp	A/G	0.000153787	0.00876755	intron-variant, missense, downstream-variant-500B	RNF212	GRCh38.p7	4:1093890	GCCCGTGTTGTGCTG[A/G]CCCAGTGTTCTTGGG	285498
rs748280770	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1076689	TACACACATCCACTC[C/T]AGGGTGACAAGGCGT	285498
rs748298415	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1094777	CTGATCTGGTGGGGA[C/G]GGCTCCCAAACCTGA	285498
rs748319126	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1106186	AAGAAAGAGCCCACA[C/T]GGTCTGTGATGGTTT	285498
rs748323630	snp	A/T			intron-variant	RNF212	GRCh38.p7	4:1069013	AGGAGTTTGAGACCA[A/T]CATGGGCAACATGGC	285498
rs748407383	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1068279	TATACTCATCGACAG[C/G]GTCCGGAAGAAAGCC	285498
rs748503752	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1064463	ACCACAGACTGGGTG[C/G]CTTACACAACAGAAG	285498
rs748545090	snp	A/T			intron-variant	RNF212	GRCh38.p7	4:1075448	GAGCAGGCGCGTTGC[A/T]GGGCGAGCAGGCAAG	285498
rs748569740	snp	A/G/T	4.95973e-05	0.00497962	intron-variant	RNF212	GRCh38.p7	4:1090751	CTAAAGGTCAAAAAA[A/G/T]TTCAAGTGGCAATGA	285498
rs748570007	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1107550	CCGCCTCCCGGGTTC[A/C]CGCATTCTCCTGCCT	285498
rs748579338	snp	C/T			intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1112294	GGCTGGTTGTAGGGC[C/T]GCATTCACTAAGGCT	285498
rs748669250	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1111357	TGGCTGTCTTGAGTT[C/T]CAGACCCACATGTGC	285498
rs748719440	snp	G/T	1.72621e-05	0.00293781	missense, upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant	RNF212, LOC105374344	GRCh38.p7	4:1113432	CCTGTGGGGCGGCTG[G/T]AAGCAGCGATTACAG	285498
rs748722217	in-del	-/AAAAA			intron-variant	RNF212	GRCh38.p7	4:1063695	GTGAGACTCAGTCTC[-/AAAAA]AAAAAAAAAAAAGAA	285498
rs748734840	snp	C/T	1.76005e-05	0.00296647	intron-variant	RNF212	GRCh38.p7	4:1081642	GATGGAGAAAAGGTA[C/T]TGAATTAAATCATAA	285498
rs748745190	snp	C/T			synonymous-codon, utr-variant-3-prime, intron-variant, nc-transcript-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1073012	AGCATATATTGGAAG[C/T]GTTTTAGAGTTGGTG	285498
rs748826358	snp	A/G	1.65743e-05	0.00287869	synonymous-codon, utr-variant-5-prime, intron-variant, nc-transcript-variant	RNF212	GRCh38.p7	4:1108373	AACTGTACGACAAGG[A/G]GCTTTACAAATCAAG	285498
rs748874662	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1109463	GGAGGACATCAGGTC[C/T]AAACCTGAACAAGCC	285498
rs748907848	in-del	-/C			intron-variant	RNF212	GRCh38.p7	4:1109749	TGACCCACCACAGAA[-/C]CAACCCACTTCACGC	285498
rs748961181	snp	A/G	5.19359e-05	0.00509561	synonymous-codon, utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1072925	AAACACAACAGACAC[A/G]GCGGGTGTTCTGAAC	285498
rs749017517	in-del	-/TTTTC			intron-variant	RNF212	GRCh38.p7	4:1099634	AATCACAAACGAATG[-/TTTTC]TTTTCGTATTTAATT	285498
rs749028600	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1057361	TTTAGCGAGACCACC[A/G]GACCTTTGAACACAC	285498
rs749036077	in-del	-/ATT			intron-variant	RNF212	GRCh38.p7	4:1083945	TTCCACATTTTGTGC[-/ATT]TTTTTTTTTTTTTTT	285498
rs749052168	in-del	-/TCCAATATTGCGGCTTACGAGATTCGG	1.67416e-05	0.00289318	intron-variant	RNF212	GRCh38.p7	4:1073696	AACAATGGGTAAAAT[-/TCCAATATTGCGGCTTACGAGATTCGG]ACTCCCACTGTCTGT	285498
rs749063976	snp	C/G	1.64743e-05	0.00287	missense, intron-variant, nc-transcript-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1073025	AGTGTTTTAGAGTTG[C/G]TGAGTTCCCCGTGCC	285498
rs749143237	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1099983	CCACTGCCGCTAGGC[A/G]GGAACGGGGTTCTCT	285498
rs749176648	in-del	-/TTTC			intron-variant	RNF212	GRCh38.p7	4:1077393	TTAGCCTGCCAGTCT[-/TTTC]TTTCTTTTTTCTTTT	285498
rs749202014	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1063076	ATAAAGGTAAAGCTA[C/T]GTCCAACATTCATGG	285498
rs749203397	snp	A/T			intron-variant	RNF212	GRCh38.p7	4:1088536	GCGACCATGCAGTAG[A/T]AAAGAAAAACCCATT	285498
rs749217008	snp	A/C	1.6489e-05	0.00287128	intron-variant	RNF212	GRCh38.p7	4:1096745	CATCACGGAACCAAG[A/C]CACACCCCTCACAGC	285498
rs749290065	snp	G/T			intron-variant	RNF212	GRCh38.p7	4:1062199	GAAGTGTGCTGACCA[G/T]TATCTCTTATGAATA	285498
rs749405962	snp	A/G	1.65693e-05	0.00287826	intron-variant	RNF212	GRCh38.p7	4:1079719	TGAAAGGCTTTGAGT[A/G]AGCCCAGGACTTACC	285498
rs749454300	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1085161	TGTGACTATTCAACG[C/T]GTCTCGTAGAATCTA	285498
rs749467344	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1098523	TGAGACCCAACAGAG[C/G]GGAGACCTGGCTCTG	285498
rs749502684	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1097502	CCCAGCTACTCAGGA[C/G]GCTGAGGCAGGAGAA	285498
rs749564854	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1059269	GAGGATGCTGCCTGC[A/G]GGAGGCATCGTAACT	285498
rs749603243	snp	A/G	3.33317e-05	0.00408224	intron-variant	RNF212	GRCh38.p7	4:1090879	CTGACACAGATCCAC[A/G]GTCTCTGTGGCTGGA	285498
rs749621619	snp	C/T			intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1056756	CTCCATGGCTGCCCT[C/T]GGCACACACTCAGTT	285498
rs749643469	in-del	-/C	4.9899e-05	0.0049947	intron-variant	RNF212	GRCh38.p7	4:1108305	TAAAAGGAAATATGA[-/C]TGTGATTAAGATGCA	285498
rs749693476	snp	A/C	3.34163e-05	0.00408742	utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant	RNF212, LOC105374344	GRCh38.p7	4:1113497	AGCGGCGAGGCCGGG[A/C]CCACGCGAAGCCCAC	285498
rs749698138	snp	C/T	1.65228e-05	0.00287422	intron-variant	RNF212	GRCh38.p7	4:1090758	TCAAAAAAATTCAAG[C/T]GGCAATGAATCAATT	285498
rs749701432	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1104738	GCTCAGATGCTGGGG[C/T]AGCATGTGGCCCCTT	285498
rs749713132	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1065003	GGCTGAATCATAGCC[C/T]ACTGTACGGAGACAC	285498
rs749717035	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1074484	CTTTAATCCACAGGC[C/G]CTTCCAGTACACCGT	285498
rs749751094	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1094847	AAAGGACCCCAGAAC[C/T]GACTGAGACCACTTT	285498
rs749766291	snp	C/G			upstream-variant-2KB, intron-variant	RNF212, LOC105374344	GRCh38.p7	4:1114655	GGGCTGGGTGCGGTA[C/G]CTCACGCCTGTAATC	285498
rs749806478	snp	C/T	1.69143e-05	0.00290807	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1073219	ATGCAGGAGACAGCG[C/T]GTGGGGAGATGGCCT	285498
rs749848980	snp	C/T	1.93452e-05	0.00311002	utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant	RNF212, LOC105374344	GRCh38.p7	4:1113487	GGGCGACCGCAGCGG[C/T]GAGGCCGGGCCCACG	285498
rs749853063	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1076599	TCTGCTCAGGCTGAG[A/G]GTTACCAGGAGCACC	285498
rs749926314	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1085452	TGCAACACCCATTCA[C/T]AGCAGTGCCTTTATA	285498
rs750032678	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1084452	AAATACATTGTGGCC[A/G]GGTGCAGTGGCTCAC	285498
rs750041377	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1090848	TAAAATCTGAAAAGA[C/T]CATAGGTTTCAGCTG	285498
rs750066240	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1059668	TCCTTTCCTCATAGC[C/G]GTTGCCTCCTCATCC	285498
rs750089566	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1097240	AGTCACCACTATGTA[C/G]TCACAAGTACATGTC	285498
rs750109876	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1077521	TATAGGCGTGAGCCC[A/G]ACATGCCTGCTGCCT	285498
rs750156244	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1058899	CCCCCGCCTCTCCCA[A/G]GCCTTGGCTCCTGCT	285498
rs750183731	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1081210	CTGCAGGATGGAGTG[C/T]TCTGATTGGCCACCT	285498
rs750216019	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1091608	ACAAGCAGGAGGGAG[C/T]GGCCTTGTCTGCCCA	285498
rs750259221	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1090705	TCCCCTTTGAGAGCA[A/C]GGTGTTAATTAACAA	285498
rs750268190	snp	A/C/G	0.000100076	0.00707319	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1073198	TAGATGTGGCCCTGC[A/C/G]GGAAGATGCAGGAGA	285498
rs750286147	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1107337	ATTACAGGTGTGAGC[A/C]ACTGCGCCTGGCCGA	285498
rs750286157	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1064751	CCCATCTCTATAACT[C/G]TTTTCATTTTGTGAA	285498
rs750317464	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1103090	TATGGAACTTACAGA[A/C]ATGAAAAATATGAGT	285498
rs750407168	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1076171	ATGTGAAGGCAGACT[C/G]TCCCTTGCCTTCCCG	285498
rs750434658	snp	G/T			intron-variant	RNF212	GRCh38.p7	4:1064151	TTAAGAAACATAAGT[G/T]TAATTCAGGAAATAA	285498
rs750462993	snp	G/T	0.000166531	0.00912346	missense, intron-variant, nc-transcript-variant	RNF212	GRCh38.p7	4:1081602	GTGCTGAAAGCTGTT[G/T]GTTGTGATGATCTCA	285498
rs750556734	snp	C/T	4.96298e-05	0.00498121	intron-variant	RNF212	GRCh38.p7	4:1108332	TGCAGATACGACACA[C/T]TTCAACTTACATGCT	285498
rs750617650	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1061841	ATACAAGAATCCAGA[C/G]TTGCTGGGACAAATA	285498
rs750699574	snp	G/T	0.000946671	0.0217357	intron-variant, synonymous-codon, downstream-variant-500B	RNF212	GRCh38.p7	4:1093826	GTCCTGGATGGTGTT[G/T]CCCTGGGCCTCTGGC	285498
rs750792868	snp	C/G			intron-variant, missense	RNF212	GRCh38.p7	4:1094344	GACATCCAAGGAGGC[C/G]AGAAGTGCCACTCAG	285498
rs750810013	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1094451	GCTGACTGGGAGGAG[A/G]GTCAGGAAGAAACAG	285498
rs750820675	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1068754	GTCTATTAGCAATGA[A/G]TTCTGTTTCTGTTAC	285498
rs750874171	in-del	-/T			intron-variant	RNF212	GRCh38.p7	4:1107458	TCTGGGGACTTACAC[-/T]TTTTTTTTTTTTTTT	285498
rs750880705	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1105215	TGTGTGTGTAAAAAC[C/T]GGCCCGGTCTAGCTT	285498
rs750888993	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1079911	CCTCTCCAGGACAGA[A/G]GCCGCTGGCCGGCCC	285498
rs750910217	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1067639	GAAGGCTGAGGTGGA[C/T]GGATGGCTTGAGGCC	285498
rs750931193	snp	A/G			upstream-variant-2KB, intron-variant, utr-variant-5-prime	RNF212, LOC105374344	GRCh38.p7	4:1113786	GCCTGGGTGGCGGGC[A/G]CGGGGAATGGCGGCT	285498
rs750937143	snp	C/T	0.000616143	0.0175411	intron-variant, utr-variant-3-prime	RNF212	GRCh38.p7	4:1094053	AGAAGCAAGGAAGCT[C/T]CCAGAGGAGGACAGT	285498
rs750940422	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1087790	GACAGTGAGTTCTCA[C/T]GAGATCTGATGGTTT	285498
rs751052781	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1103216	AATTAGGAACTTTAA[A/G]CAGTTCGATGTCTAA	285498
rs751140915	snp	C/T			upstream-variant-2KB, intron-variant	RNF212, LOC105374344	GRCh38.p7	4:1114426	GAGCGCTCCCGGTAG[C/T]TACGGGCCAAGTGAC	285498
rs751163052	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1076230	TAGGCTCTGCTTCTC[C/T]TCCTCCCCAGTGCCA	285498
rs751182578	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1075746	TGGGGCAGTCACTCA[C/T]CTCACTGCAGCCTCA	285498
rs751208958	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1085636	CTCTCCCAGGCCCCT[C/T]CCACTGCCTCAGCAA	285498
rs751306696	snp	A/G/T	3.30689e-05	0.00406615	stop-gained, missense, utr-variant-5-prime, intron-variant, nc-transcript-variant	RNF212	GRCh38.p7	4:1108350	CAACTTACATGCTTT[A/G/T]AAAGCAAAACTGTAC	285498
rs751322072	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1109144	TCCCAAGTGACTGGG[C/T]GTACAGGTGCCTGCC	285498
rs751408717	snp	C/T	3.37109e-05	0.0041054	intron-variant	RNF212	GRCh38.p7	4:1073704	GTAAAATTCCAATAT[C/T]GCGGCTTACGAGATT	285498
rs751417334	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1057126	CATCTCTGAGAACCT[C/T]GGAGCAGCACGCACA	285498
rs751430977	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1088642	CCAGGGCATGTGAGA[A/G]ATCTTCACAGCAGCC	285498
rs751443939	snp	C/T	1.99527e-05	0.00315847	intron-variant	RNF212	GRCh38.p7	4:1108456	ACTACTACTTTTAAA[C/T]ATGTATACATGCAGA	285498
rs751478670	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1104265	GCGGACATGCGAAGA[C/T]GAATGTAGGCCAACT	285498
rs751479078	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1092751	GGCCCCAAGGAAGAG[C/T]TGCCCGGTGCTCACG	285498
rs751511830	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1057225	ACAACCCAGGCCAGC[A/G]GGGACGGGAGGTGGG	285498
rs751519908	in-del	-/CAAA			intron-variant	RNF212	GRCh38.p7	4:1077228	AGTGAGACTCTGTCT[-/CAAA]CAAACAAACAAACAA	285498
rs751569272	snp	C/G			intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1056554	AAAAAATAAGGTGGG[C/G]AGAAGAGTTTATTCA	285498
rs751645312	snp	C/G	3.33089e-05	0.00408085	missense, intron-variant, nc-transcript-variant	RNF212	GRCh38.p7	4:1085906	CTTACCTTTGTAGTT[C/G]TTCTATCTGCAGCAC	285498
rs751647382	snp	C/G	1.64882e-05	0.00287121	missense, utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1072976	CTGCTGGAACGGAAA[C/G]AAGACGGCCCTTTGT	285498
rs751684242	in-del	-/AC	1.93868e-05	0.00311336	frameshift-variant, utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1072912	ATTGGCAAAGAGGAA[-/AC]ACAACAGACACAGCG	285498
rs751745441	snp	A/T			intron-variant	RNF212	GRCh38.p7	4:1101327	TGGTAGACAATACTG[A/T]GCAGAATTTTTCTCA	285498
rs751841493	snp	G/T	4.94181e-05	0.00497057	missense, stop-gained, intron-variant, nc-transcript-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1073074	GGAGGAGCAGCCAGT[G/T]AGGACAGACGTCTAT	285498
rs751852111	snp	A/G	1.64735e-05	0.00286993	synonymous-codon, nc-transcript-variant	RNF212	GRCh38.p7	4:1096797	AGTACTTCTTACACA[A/G]ACTGTCTATGCTCAT	285498
rs751891898	snp	A/T			intron-variant	RNF212	GRCh38.p7	4:1062830	GAGAATCCACAAAAA[A/T]AATCCCCAGAGCTCA	285498
rs751921269	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1111228	TCCTTCAACAAATGC[C/T]CTTTCCAACAAGATA	285498
rs751936580	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1084543	AAGACTAGCCTGGGT[A/G]ACATAGTGAGACCCC	285498
rs751937530	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1062762	TTGGAAAGGAAAAAG[C/T]AAAACAACCTCCACT	285498
rs751940372	snp	A/T	0.000392503	0.0140035	intron-variant, utr-variant-3-prime	RNF212	GRCh38.p7	4:1094058	CAAGGAAGCTCCCAG[A/T]GGAGGACAGTCTTGG	285498
rs751983896	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1059764	ACGATGGCAGGTATC[C/T]TTTGTTAAGTAACTT	285498
rs752027512	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1084184	TCAAACTCCCGACCT[C/G]AGGTAATCTGCCCAC	285498
rs752048664	in-del	-/TTTATCTCATCCTAA			intron-variant	RNF212	GRCh38.p7	4:1066056	CCATCCTAATGGCTG[-/TTTATCTCATCCTAA]TTTATCTCATCCTAA	285498
rs752050280	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1097300	TTAAGAAAGGACACA[A/G]GTTTAAGAAACAGCG	285498
rs752064656	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1069580	TCCTGGAGGAATCAC[A/G]TGACCAAAGTGAAGA	285498
rs752161891	in-del	-/C	0.000397193	0.0140868	intron-variant	RNF212	GRCh38.p7	4:1090849	AAAATCTGAAAAGAT[-/C]ATAGGTTTCAGCTGC	285498
rs752280435	snp	A/G	0.000157023	0.00885928	intron-variant, synonymous-codon, downstream-variant-500B	RNF212	GRCh38.p7	4:1093787	GGTCCTGCTGGGATG[A/G]AGCAGGGTGAGGGGG	285498
rs752317286	snp	G/T			intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1092836	GCAGTCGGGGGAGAA[G/T]GCAGGTCACTCACGC	285498
rs752342426	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1077345	CCTCAGCAATAATTT[C/T]CAACAGTAGCACCTA	285498
rs752354919	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1078177	CTGTGTCGCACAACC[C/T]GAAGCAACACATAAA	285498
rs752382096	snp	A/G			intron-variant, upstream-variant-2KB	TMED11P, LOC105374344, RNF212	GRCh38.p7	4:1115648	TCAGGAATTTGACCT[A/G]TTCGTATATTTTATT	285498
rs752386784	snp	A/T	1.65548e-05	0.002877	synonymous-codon, intron-variant, missense, nc-transcript-variant	RNF212	GRCh38.p7	4:1079655	TACTTTTCTAATCGG[A/T]GAAGGAGAGAGATCA	285498
rs752421038	snp	A/G	1.7426e-05	0.00295173	synonymous-codon, upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant	RNF212, LOC105374344	GRCh38.p7	4:1113393	GTACACGTGCCCGCA[A/G]TTGGTGAGGCTGAAG	285498
rs752461693	snp	A/G			intron-variant, utr-variant-5-prime	RNF212	GRCh38.p7	4:1099796	ATCAACCCTGGTGCA[A/G]AGCAATCGAGTCCAC	285498
rs752497427	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1110100	CCGACTCATAAAAAT[C/T]GAAAAGTTCTTACAA	285498
rs752510935	snp	C/T	3.93275e-05	0.00443421	intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1113318	GACCCCCTTGCCGCT[C/T]CCCTCCCCTCTCCAG	285498
rs752528075	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1083220	AGGATATCAGGTAAG[A/G]AAAATAAAAAGGCTG	285498
rs752543934	snp	C/G			intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1073535	TTGATTAAACATGAC[C/G]TTTCAGGGAATGCAT	285498
rs752561082	snp	A/G	1.66502e-05	0.00288527	synonymous-codon, intron-variant, nc-transcript-variant	RNF212	GRCh38.p7	4:1085918	GTTGTTCTATCTGCA[A/G]CACTGACTTCCTAAG	285498
rs752588289	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1103906	AAAAAAAGGAAGCGC[A/G]TAAGGAATAGAAAGA	285498
rs752631912	snp	A/G			utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1072781	GAGGGCTTCCACATA[A/G]ATGACAAAGGAATAA	285498
rs752691442	in-del	-/CCAA			intron-variant	RNF212	GRCh38.p7	4:1060244	CAGTGCTCAAGAGAG[-/CCAA]CCAAGTGTGGGCCAT	285498
rs752704523	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1075441	CAAGGGGGAGCAGGC[A/G]CGTTGCAGGGCGAGC	285498
rs752755246	in-del	-/AAAA			intron-variant	RNF212	GRCh38.p7	4:1063696	TGAGACTCAGTCTCA[-/AAAA]AAAAAAAAAAAAGAA	285498
rs752780615	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1081741	ACTGGGTTTGCAAAC[A/G]GCATTTCACATGAAT	285498
rs752786305	snp	A/G	4.94523e-05	0.00497229	missense, intron-variant, downstream-variant-500B, nc-transcript-variant	RNF212	GRCh38.p7	4:1073154	GGCTTAGACAAGGTC[A/G]ACCATGGGATGAAAC	285498
rs752839215	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1066254	TTTGCATTTCTCTAA[C/T]GATGAACGATGAGTA	285498
rs752866811	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1081118	GGGCTGTCAGCTGCC[A/G]GGCACTGGAACGCCA	285498
rs752959828	snp	A/G	1.6473e-05	0.00286988	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RNF212	GRCh38.p7	4:1096828	GAAGAATGCCTGGAT[A/G]TCTGCGTCGGTCTGA	285498
rs752991256	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1059480	GGAGGCCACGGTGAG[C/G]ACACTTCTGATATGA	285498
rs752994226	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1090926	AGGAGGCTGGAGGGA[C/T]TCTCAGGAGAGCTCA	285498
rs753010173	in-del	-/AC	4.94214e-05	0.00497074	frameshift-variant, intron-variant, downstream-variant-500B, nc-transcript-variant	RNF212	GRCh38.p7	4:1073118	GAACCTCTGGAAATG[-/AC]ACACTCTCCGGGCAC	285498
rs753051451	snp	A/C	0.000185374	0.00962562	intron-variant, missense	RNF212	GRCh38.p7	4:1099731	AGCGTGACTGAAGGC[A/C]TTTGCTGCGTCTGAC	285498
rs753108043	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1088091	ACTGGGTAATGGGCA[A/G]AAGTTGGAACAATTT	285498
rs753181110	in-del	-/TT			utr-variant-3-prime, intron-variant	RNF212	GRCh38.p7	4:1071573	ATATACACAGGACTC[-/TT]AAAACTCAACAATAA	285498
rs753187826	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1098871	ATCTAAGGTATATTA[C/T]AAATACACAGATGCC	285498
rs753197988	snp	A/G			synonymous-codon, intron-variant, nc-transcript-variant	RNF212	GRCh38.p7	4:1085949	GGATTCTTCCAACCT[A/G]GAAATCTAAACATAA	285498
rs753206844	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1059819	GAAATTGTAGGCTGG[C/G]TGTGGTGGCTCATGC	285498
rs753261112	snp	C/G			downstream-variant-500B, intron-variant	RNF212	GRCh38.p7	4:1071435	TTCTGTTCTGTGAAA[C/G]ATAATGTCAAGAGAA	285498
rs753268507	snp	G/T			intron-variant	RNF212	GRCh38.p7	4:1108526	ACTTACAGGTTTTCA[G/T]GTTCTGACAGGATGA	285498
rs753359200	in-del	-/G			intron-variant, upstream-variant-2KB	TMED11P, LOC105374344, RNF212	GRCh38.p7	4:1115615	ATAAAAGATGGTTTT[-/G]TATTTTGGTGTAAAA	285498
rs753403200	snp	A/G			intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1058181	TCTCTCTGGTGAGTG[A/G]GATGATGAGCAGTTT	285498
rs753411735	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1058778	AGGGGCCCTCGGCCC[A/G]TGGGCTCTGCGAGGG	285498
rs753455364	in-del	-/TTGT			intron-variant	RNF212	GRCh38.p7	4:1108727	TTTTGAGACAAGGTC[-/TTGT]TCTGTTGCCCAGGCT	285498
rs753458496	in-del	-/TACTTTTGAAGTTTTTAGCAACAGGGCAAATGCC			intron-variant	RNF212	GRCh38.p7	4:1057714	GCAGTCACCACGTGG[lengthTooLong]TACGTTATATCTTAG	285498
rs753462018	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1080627	AATTAAAACTCCTCA[C/T]GGGAAACCTGCCTGG	285498
rs753493091	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1067180	AAATATAGTCACATT[A/G]GAGGTTAGGGCTTCA	285498
rs753499745	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1068504	CCTCGCTCTTCCTTT[A/G]TGCTTATTATCCTCT	285498
rs753561219	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1089822	CTGTTAATGTAAGAC[A/G]TGCCTTGCTTCCCCT	285498
rs753564383	snp	C/T	1.65002e-05	0.00287225	missense, intron-variant, nc-transcript-variant	RNF212	GRCh38.p7	4:1090814	CTAACAATCTCTTCC[C/T]GTGTTTTTCTTGAAA	285498
rs753604865	snp	A/G	1.64749e-05	0.00287005	synonymous-codon, missense, intron-variant, downstream-variant-500B, nc-transcript-variant	RNF212	GRCh38.p7	4:1073120	ACCTCTGGAAATGAC[A/G]CACTCTCCGGGCACA	285498
rs753659568	snp	A/G	6.66878e-05	0.00577403	missense, intron-variant, nc-transcript-variant	RNF212	GRCh38.p7	4:1085953	TCTTCCAACCTAGAA[A/G]TCTAAACATAATTAC	285498
rs753667145	in-del	-/CCACG	0.000540248	0.0164266	intron-variant, frameshift-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1093544	CAGAGCCTGTGACCT[-/CCACG]GCCCATGCCGGAAGC	285498
rs753684807	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1091791	GGGATGACAGCCTCG[C/T]GGTTTCCTGGCTGCT	285498
rs753707216	snp	A/G	1.64988e-05	0.00287213	missense, intron-variant, downstream-variant-500B, nc-transcript-variant	RNF212	GRCh38.p7	4:1073166	GTCAACCATGGGATG[A/G]AACAGAAAGAAGCTG	285498
rs753767139	snp	A/C			intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1111833	AAATCTGCAAACAAC[A/C]CAAAGGGCCATGGAC	285498
rs753770708	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1084372	GTCCACATAAGGTCT[C/T]CGTTGCAATGCGTTT	285498
rs753856988	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1098924	CATGGACCAGAAATG[A/G]GAGCAACTGAAGAAG	285498
rs753865016	snp	C/T			utr-variant-3-prime, intron-variant	RNF212	GRCh38.p7	4:1072492	GATGGGGGAGCTGTG[C/T]GTGTGTGGAGTCATG	285498
rs753913868	in-del	-/GAGACCTCAGCACGG			upstream-variant-2KB, intron-variant	RNF212, LOC105374344	GRCh38.p7	4:1114199	GTGGCCGCTGGCGCA[-/GAGACCTCAGCACGG]GAGGCCTGAGCCTGC	285498
rs753949121	snp	A/T			intron-variant	RNF212	GRCh38.p7	4:1108761	GATCTGCAAGTGGCA[A/T]GATCACAGCTCACTG	285498
rs753969971	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1105199	GCTACTCCTTTCCAC[A/G]TGTGTGTGTAAAAAC	285498
rs753971612	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1082572	AACCACTGGGGCCTC[C/T]GCTCTGAGTCACCTC	285498
rs753992267	snp	A/G	1.6585e-05	0.00287962	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1073558	GAATGCATTTTAATC[A/G]ATGCATGTATCGGTC	285498
rs753994635	in-del	-/AC			intron-variant	RNF212	GRCh38.p7	4:1075533	CCCACCATGGCAAAG[-/AC]AGCACCAGCCACCAG	285498
rs754002901	snp	A/G	1.65905e-05	0.0028801	intron-variant	RNF212	GRCh38.p7	4:1108315	TATGACTGTGATTAA[A/G]ATGCAGATACGACAC	285498
rs754141065	in-del	-/AAAC			intron-variant	RNF212	GRCh38.p7	4:1083643	CTCTGTCTCAAAAAC[-/AAAC]AAACAAACAAACAAA	285498
rs754208746	snp	A/G			intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1058288	TGCGGGGGTTAGAAC[A/G]CAGTGAAGAAGGTGC	285498
rs754263150	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1078443	CCCACCAGGACAGAC[A/G]ACGGGAGAGCCGGGC	285498
rs754263617	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1077978	TGCCAAGGAACTGGC[A/G]TTTCTCTTTCACGGA	285498
rs754350981	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1088938	AGATGTATGGAAATG[A/C]CTGGATGTCCAGGCA	285498
rs754353473	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1097777	GAGCTAGAATCGCTT[A/G]AGCAGTCCAAAGAAA	285498
rs754416447	in-del	-/CTG			intron-variant	RNF212	GRCh38.p7	4:1065940	GAGTGCAGTGATGCA[-/CTG]ATCATAGTTCACTGC	285498
rs754438865	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1088243	TCAGATGGAGATAAG[C/G]AATTTATTGGGACTG	285498
rs754459865	snp	A/T			intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1056562	AGGTGGGGAGAAGAG[A/T]TTATTCACTAAAATG	285498
rs754499821	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1103346	CCCCATCTTACAAAA[A/C]ATTTTCCAGAGAAGA	285498
rs754545329	snp	G/T	0.00279952	0.0373085	intron-variant, missense, downstream-variant-500B	RNF212	GRCh38.p7	4:1093554	GACCTCCACGGCCCA[G/T]GCCGGAAGCCTGAGA	285498
rs754583518	snp	A/C			upstream-variant-2KB, intron-variant	RNF212, LOC105374344	GRCh38.p7	4:1114532	TATTGATTACATGTT[A/C]ACATGATATTTTTGA	285498
rs754636575	in-del	-/T/TT			intron-variant	RNF212	GRCh38.p7	4:1083947	CACATTTTGTGCATT[-/T/TT]TTTTTTTTTTTTTTT	285498
rs754642692	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1059268	TGAGGATGCTGCCTG[C/T]GGGAGGCATCGTAAC	285498
rs754657983	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1102262	GTTTTTGAAAATACA[C/G]TCATCCTTCAGTATA	285498
rs754672432	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1076276	CAGGCCTGGAGCAGC[A/C]AGGGTGGAGGAGGAA	285498
rs754697971	snp	C/G			utr-variant-3-prime, intron-variant	RNF212	GRCh38.p7	4:1072552	CAATTTTTCTGTGAA[C/G]CTAAAACTGCTCTAA	285498
rs754741278	in-del	-/ACACAC			intron-variant	RNF212	GRCh38.p7	4:1107389	AGGTAAATCACAATA[-/ACACAC]ATAGAATAGGTACCA	285498
rs754814091	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1109182	CAGGCTAATTTTTGT[A/G]TTTTTAGTAGAGACA	285498
rs754876408	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1082660	CAGCCTGTGTCCCGG[C/T]CCGACATACAAGTTC	285498
rs754891292	snp	C/T	1.66788e-05	0.00288775	intron-variant	RNF212	GRCh38.p7	4:1085868	TGGGTGCCTCGACTG[C/T]GCACTCACGGGGGGT	285498
rs754913149	snp	C/T	7.75074e-05	0.00622476	synonymous-codon, utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1072886	AAATCAAAATGACTT[C/T]TTCCTTTCAAATTGG	285498
rs754935736	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1057137	ACCTCGGAGCAGCAC[A/G]CACACCCCCGCCCGG	285498
rs754959605	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1092768	GCCCGGTGCTCACGC[A/G]TGCTTTGCCCGCATC	285498
rs755019244	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1080955	AGATGGGGCAGACAC[A/G]AGCCACAGGACATGT	285498
rs755051512	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1068923	ATAGAAATCTATGAA[C/T]ATGGCTGGACGCAAT	285498
rs755053468	snp	C/T			upstream-variant-2KB, intron-variant	RNF212, LOC105374344	GRCh38.p7	4:1114500	GGCCTCGTATGAAAA[C/T]CTTCTTAGTAATTTT	285498
rs755070470	snp	G/T			missense, nc-transcript-variant	RNF212	GRCh38.p7	4:1096800	ACTTCTTACACAGAC[G/T]GTCTATGCTCATGAA	285498
rs755150189	snp	C/G	9.6251e-05	0.00693659	intron-variant, utr-variant-3-prime	RNF212	GRCh38.p7	4:1094060	AGGAAGCTCCCAGAG[C/G]AGGACAGTCTTGGGG	285498
rs755167651	in-del	-/T	1.68975e-05	0.00290662	frameshift-variant, utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1072933	CAGACACAGCGGGTG[-/T]TCTGAACGTGTCCAG	285498
rs755197037	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1089786	AAGAGTGTTTGGCAG[C/T]TCCCCCTGCCCTCTC	285498
rs755197167	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1078713	TGACAGGGACCAGCA[C/T]GGGACCAACATGGGA	285498
rs755306618	snp	C/T	1.6473e-05	0.00286988	missense, synonymous-codon, intron-variant, nc-transcript-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1073079	AGCAGCCAGTGAGGA[C/T]AGACGTCTATGCAGA	285498
rs755315032	snp	A/C			intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1112265	GGGAGCCACAGAAAG[A/C]GGCTTTGCTGTAGGG	285498
rs755344894	snp	G/T			intron-variant	RNF212	GRCh38.p7	4:1084547	CTAGCCTGGGTAACA[G/T]AGTGAGACCCCATCT	285498
rs755346314	snp	C/T	1.64735e-05	0.00286993	missense, nc-transcript-variant	RNF212	GRCh38.p7	4:1096802	TTCTTACACAGACTG[C/T]CTATGCTCATGAAGA	285498
rs755375748	snp	C/G/T	6.90793e-05	0.00587671	missense, upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant	RNF212, LOC105374344	GRCh38.p7	4:1113428	ACGTCCTGTGGGGCG[C/G/T]CTGGAAGCAGCGATT	285498
rs755382887	snp	A/G	4.968e-05	0.00498373	synonymous-codon, intron-variant, nc-transcript-variant	RNF212	GRCh38.p7	4:1079687	CTTCCATCGACTCCA[A/G]TCTGTTAAACACATA	285498
rs755384929	in-del	-/CAAAA			intron-variant	RNF212	GRCh38.p7	4:1063694	AGTGAGACTCAGTCT[-/CAAAA]AAAAAAAAAAAAAGA	285498
rs755461172	snp	A/T			intron-variant	RNF212	GRCh38.p7	4:1069581	CCTGGAGGAATCACG[A/T]GACCAAAGTGAAGAG	285498
rs755525251	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1109410	TGGAGCCCAGGGCTG[A/G]CCAGGCACTATGAGC	285498
rs755526992	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1059022	AAGGGGAGATGTGAC[A/G]ACTGAGTTCTCAAGC	285498
rs755537778	snp	A/T			intron-variant	RNF212	GRCh38.p7	4:1082762	ATTGCCAGCCCCCAG[A/T]ACAGTGCTGAGAATG	285498
rs755546028	snp	A/G	1.64953e-05	0.00287182	splice-donor-variant, intron-variant	RNF212	GRCh38.p7	4:1081417	GCAAGCAACCCACAC[A/G]CCTGTCGGGGGCTGA	285498
rs755620345	in-del	-/GTGAAGAAGGTGCTTGCGGGGGTTAGAACGCA			intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1058259	GGGGGTTAGAACGCT[lengthTooLong]GTGAAGAAGGTGCTT	285498
rs755671408	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1107338	TTACAGGTGTGAGCC[A/G]CTGCGCCTGGCCGAG	285498
rs755696258	snp	G/T			intron-variant	RNF212	GRCh38.p7	4:1086819	GGAGAGAGAATGGGG[G/T]GGGGGAGAGAGGATG	285498
rs755699569	snp	G/T			intron-variant	RNF212	GRCh38.p7	4:1057320	CACTCAAGGGCTCTG[G/T]GGGGCTGACATGGGA	285498
rs755703150	snp	C/T	0.00018949	0.00973186	intron-variant	RNF212	GRCh38.p7	4:1073713	CAATATTGCGGCTTA[C/T]GAGATTCGGACTCCC	285498
rs755722123	snp	C/T	2.66564e-05	0.00365068	intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1113338	CCCCTCTCCAGCCTG[C/T]GTTCGGGAAGCCCTG	285498
rs755779797	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1092003	GCACCTTTCCCACCT[C/T]TGCCGACGCTTCTCA	285498
rs755827374	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1100632	CAGGCTGGTCTCAAA[C/T]GCCTGACCTCAGGTG	285498
rs755853138	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1089074	GCCTAGAGAAGCCAT[A/G]AGAAGAGGGCCACTG	285498
rs755872120	snp	C/T	1.66765e-05	0.00288756	intron-variant	RNF212	GRCh38.p7	4:1085876	TCGACTGCGCACTCA[C/T]GGGGGGTGGGGCGCC	285498
rs755915540	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1110882	GGAGGAATGCACTCA[C/G]ACTACTGGAATCTGT	285498
rs755953181	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1062944	AAAAGTTACAAAACA[A/G]TTCTATTTATAGTAG	285498
rs756011191	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1089926	TTCCTTTATAAATTA[C/T]CGAATCTCAGGTTAT	285498
rs756042775	snp	A/C			intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1073545	ATGACCTTTCAGGGA[A/C]TGCATTTTAATCGAT	285498
rs756119972	snp	G/T	1.66554e-05	0.00288573	missense, intron-variant, nc-transcript-variant	RNF212	GRCh38.p7	4:1085926	ATCTGCAGCACTGAC[G/T]TCCTAAGGGATTCTT	285498
rs756131847	snp	C/G			missense, utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1072935	GACACAGCGGGTGTT[C/G]TGAACGTGTCCAGGG	285498
rs756168237	snp	A/C			downstream-variant-500B, intron-variant, utr-variant-3-prime	RNF212	GRCh38.p7	4:1071474	AAGCCACAAAATGGA[A/C]GAATATATTTTCAAG	285498
rs756311759	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1097462	ATAAAAAAATTAGCC[A/G]GGCGTGGTGACGGGC	285498
rs756323025	in-del	-/T	1.68556e-05	0.00290302	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1073215	AAGATGCAGGAGACA[-/T]GCGTGTGGGGAGATG	285498
rs756404954	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1064940	TAGCATAGCGTCCTC[A/G]ATGTTCATCCACGCG	285498
rs756471781	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1077493	CTGCCTTGGCCTCCC[A/G]AAGTGCTGAAGTTAT	285498
rs756497083	snp	C/T			upstream-variant-2KB, intron-variant	RNF212, LOC105374344	GRCh38.p7	4:1114586	GTAGCGTTGATTTTA[C/T]CCTTTCAAAAAATCC	285498
rs756530916	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1076330	GCGGGCCCAGCTGTG[C/T]CCCAGGCGCTGTCAT	285498
rs756611193	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1060733	GATGCCAGATCCACT[A/G]TGCTGTGTTCTGGAG	285498
rs756693949	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1086044	ACCTTGAATCAGAAT[A/G]TGGGTTACTCTGCAT	285498
rs756694587	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1073700	ATGGGTAAAATTCCA[A/G]TATTGCGGCTTACGA	285498
rs756702218	snp	G/T			intron-variant	RNF212	GRCh38.p7	4:1098911	AGACCAAGAGCTCCA[G/T]GGACCAGAAATGGGA	285498
rs756730786	snp	A/G	6.06729e-05	0.00550752	utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant	RNF212, LOC105374344	GRCh38.p7	4:1113494	CGCAGCGGCGAGGCC[A/G]GGCCCACGCGAAGCC	285498
rs756792510	snp	C/G			intron-variant, missense	RNF212	GRCh38.p7	4:1094322	TGGTGGACTGCAGCT[C/G]TCCGGTGACATCCAA	285498
rs756792573	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1058808	GGAGCCTGCCCGTCA[C/T]GGGGGCAGCTGTGGG	285498
rs756904285	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1073843	CTCTGCCTGCTGGTG[A/G]TAGAGGTGGTGTGGG	285498
rs756940734	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1082848	TACCTGAGCCTTCTG[C/T]GTCTGGCAGGGCCGT	285498
rs756965389	snp	A/G			intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1058236	AACGCTGTGAAGAAG[A/G]TGCTTGCGGGGGTTA	285498
rs756970384	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1065082	TTTTAGACACTGTGA[A/G]TAATACTGCTACGAT	285498
rs757007823	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1080156	CATTTGCCAAAGGCA[C/G]ACAGGAAAACATCAT	285498
rs757010489	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1096449	TCATCACGGAACCAA[C/G]CACACCCCCCACAGC	285498
rs757026058	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1088806	TCCAAGGTACAATTT[C/G]GGCTGCTGCTTCAGA	285498
rs757042078	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1101935	TCACAGAAACTGTAA[A/C]TAAAAACTTGCAAAT	285498
rs757048057	in-del	-/GCCCAGGCTGGAGCCAGCCATCA			intron-variant, frameshift-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1093543	CAGAGCCTGTGACCT[-/GCCCAGGCTGGAGCCAGCCATCA]CCACGGCCCATGCCG	285498
rs757058784	snp	G/T	1.65064e-05	0.00287279	missense, intron-variant, nc-transcript-variant	RNF212	GRCh38.p7	4:1090825	TTCCTGTGTTTTTCT[G/T]GAAATTCTAAAATCT	285498
rs757060752	snp	A/T	1.64743e-05	0.00287	missense, intron-variant, downstream-variant-500B, nc-transcript-variant	RNF212	GRCh38.p7	4:1073122	CTCTGGAAATGACAC[A/T]CTCTCCGGGCACAGG	285498
rs757204717	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1100684	AAAGTGCTGGGATTA[C/T]AGGCGTGAGCCACCG	285498
rs757253008	in-del	-/GGCACT			intron-variant	RNF212	GRCh38.p7	4:1105340	CCCACCACATCCCCA[-/GGCACT]GGCTTCAGTCTGCTC	285498
rs757283948	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1063180	CGAGATTTCAACCTG[C/T]TTTGTCAGCAGAAAT	285498
rs757301176	snp	A/G			upstream-variant-2KB, intron-variant	RNF212, TMED11P, LOC105374344	GRCh38.p7	4:1114794	GTCTCAACAACAACA[A/G]CAGCAAATTAGAATT	285498
rs757312613	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1082790	ATGCACCTGGTGCTC[A/G]GTAAACACTGGCTGC	285498
rs757323311	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1088395	TCTAAGCAGCAAAGC[A/G]TTCAAGATGTGACCT	285498
rs757337715	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1081112	AGGGCAGGGCTGTCA[A/G]CTGCCGGGCACTGGA	285498
rs757389710	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1101337	TACTGAGCAGAATTT[C/T]TCTCAGGGAAACCAC	285498
rs757395108	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1099009	TCTACACATGACAGA[C/T]ACCCCAGGATGTCCA	285498
rs757452361	snp	C/T	1.66134e-05	0.00288208	missense, intron-variant, nc-transcript-variant	RNF212	GRCh38.p7	4:1081591	AACTTTTTATTGTGC[C/T]GAAAGCTGTTTGTTG	285498
rs757621461	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1099552	AGCTGAGGCCCTCGC[A/G]TCATCAAGAAAACTG	285498
rs757801475	snp	C/T	8.10734e-05	0.00636633	intron-variant, missense, downstream-variant-500B	RNF212	GRCh38.p7	4:1093810	TGAGGGGGTGAGGTG[C/T]GTCCTGGATGGTGTT	285498
rs757803092	snp	C/T	1.64928e-05	0.00287161	missense, utr-variant-3-prime, nc-transcript-variant	RNF212	GRCh38.p7	4:1073610	TTACCCATTCGTCCA[C/T]CTTGAGGTGGACTAA	285498
rs757814155	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1064297	CCACTGGAATTCAGT[C/T]GGTGTTCACCTCAGT	285498
rs757891066	snp	A/G	0.00035057	0.0132349	intron-variant, missense, downstream-variant-500B	RNF212	GRCh38.p7	4:1093575	AAGCCTGAGAGGCAC[A/G]AGAGGCAGAGCAGAC	285498
rs757894011	snp	A/C			intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1112089	TGCACATGCCTGTAG[A/C]CCCGCTACCCTGGAG	285498
rs757910394	snp	A/G	1.66815e-05	0.00288799	utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant	RNF212, LOC105374344	GRCh38.p7	4:1113488	GGCGACCGCAGCGGC[A/G]AGGCCGGGCCCACGC	285498
rs757915655	snp	A/G			intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1111781	GATCACCGAAGACAG[A/G]AGCAAGAAGATTCAC	285498
rs757938526	snp	C/G	0.000649984	0.0180158	intron-variant, missense, downstream-variant-500B	RNF212	GRCh38.p7	4:1093544	CAGAGCCTGTGACCT[C/G]CACGGCCCATGCCGG	285498
rs757958217	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1075024	TTAGAGAAAATCTCC[A/G]CAGAGCGTTCAAGTG	285498
rs758053334	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1111201	TCTTTTTTACCTGAC[A/G]TCTTCTTTACCTCCT	285498
rs758100438	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1081808	CCTGCTCCTCCCTAG[A/C]GCTGAAGCCAAGTGA	285498
rs758108691	snp	A/G	3.31192e-05	0.00406921	intron-variant	RNF212	GRCh38.p7	4:1090850	AAATCTGAAAAGATC[A/G]TAGGTTTCAGCTGCT	285498
rs758184597	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1069961	TGTGTCAGCGTGGAC[A/G]CCTAGCCTGAATTAC	285498
rs758286862	snp	A/G			utr-variant-3-prime, nc-transcript-variant	RNF212	GRCh38.p7	4:1056385	GGAAGGGGGCAGAGC[A/G]GGTGGCTGGGTGCTC	285498
rs758330834	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1091780	CCAGGACAGCAGGGA[C/T]GACAGCCTCGCGGTT	285498
rs758371556	snp	A/T	1.65288e-05	0.00287474	intron-variant	RNF212	GRCh38.p7	4:1081521	ACAGTGTGACTCAGC[A/T]ACATGCATCTCTATT	285498
rs758420912	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1090708	CCTTTGAGAGCAAGG[C/T]GTTAATTAACAAGTC	285498
rs758462121	snp	C/G	0.000185408	0.00962652	intron-variant, utr-variant-5-prime	RNF212	GRCh38.p7	4:1099817	TCGAGTCCACAAGGT[C/G]CGACGGCGCAAGCGG	285498
rs758462806	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1078579	TCTTTTCCTGGGCTG[A/C]CAAAGTTTACTACTG	285498
rs758550889	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1089022	AGAAGGGAAATGTGC[A/G]GTGGTTGTTCCCACA	285498
rs758566453	snp	C/T	1.66902e-05	0.00288874	synonymous-codon, intron-variant, nc-transcript-variant	RNF212	GRCh38.p7	4:1081607	GAAAGCTGTTTGTTG[C/T]GATGATCTCATACTA	285498
rs758721986	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1060887	TGAGGGGTCCAGGAC[A/C]TGCCGTTCAACAACT	285498
rs758753698	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1097255	GTCACAAGTACATGT[C/T]GAGTTATTTAAAAAG	285498
rs758776452	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1082250	ACCCTGGACTGATCT[C/G]CACGATGGCCAGTAG	285498
rs758783223	in-del	-/AT			intron-variant	RNF212	GRCh38.p7	4:1079762	AGTTGAAATACACAC[-/AT]GACGAGATGATGTGT	285498
rs758804936	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1109297	ATAGGCATGAGCCAC[C/T]ATGCCCAGCCTATGA	285498
rs758870739	snp	C/G	0.00126422	0.02511	intron-variant, utr-variant-3-prime	RNF212	GRCh38.p7	4:1094054	GAAGCAAGGAAGCTC[C/G]CAGAGGAGGACAGTC	285498
rs758924823	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1100085	CTTGGGGCGCCAGGC[C/T]TACACAGGACTTCCT	285498
rs758986209	snp	C/T	3.30857e-05	0.00406716	intron-variant	RNF212	GRCh38.p7	4:1079599	AAATGGGAAATGCCA[C/T]ACGTCTGGTATACAG	285498
rs759033688	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1077248	CAAACAAACAAACAA[A/C]AAACAAAAAGCAAAA	285498
rs759065878	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1078141	TAAAGGGCTCGGAAC[A/G]GTGCTTGCCAATGAG	285498
rs759081696	snp	C/T	1.67016e-05	0.00288973	synonymous-codon, utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1072940	AGCGGGTGTTCTGAA[C/T]GTGTCCAGGGTGCCC	285498
rs759325756	snp	A/C	8.868e-05	0.00665824	intron-variant, missense, downstream-variant-500B	RNF212	GRCh38.p7	4:1093746	TCAAGCAACTTCTGG[A/C]CCCAAGGGGACTTGG	285498
rs759366913	snp	A/T			intron-variant, missense, downstream-variant-500B	RNF212	GRCh38.p7	4:1093963	GCACCTCCTTGGAGG[A/T]TGTGGCTGGGCATAA	285498
rs759406169	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1104819	CGTGTCTGCATCCTC[A/G]CCATGACCTGACATC	285498
rs759480910	snp	C/T			intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1112680	GACTCGTGGCCCGAC[C/T]CCTGTGTCCCCCTCA	285498
rs759531222	snp	A/G			downstream-variant-500B	RNF212	GRCh38.p7	4:1056007	CCCGCTGAAGCCGGC[A/G]TCACAGGCCCGCTGT	285498
rs759535226	snp	A/G	3.33034e-05	0.00408051	missense, intron-variant, nc-transcript-variant	RNF212	GRCh38.p7	4:1085911	CTTTGTAGTTGTTCT[A/G]TCTGCAGCACTGACT	285498
rs759588923	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1091241	AGCGAGACCCACAGA[A/G]CTGGCAGAGGCCTGG	285498
rs759658531	in-del	-/GCTGCCCAGGCTGGAGCCA	0.000351556	0.0132535	intron-variant, frameshift-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1093538	CTGGGCAGAGCCTGT[-/GCTGCCCAGGCTGGAGCCA]GACCTCCACGGCCCA	285498
rs759663532	snp	C/G	3.60802e-05	0.00424721	utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant	RNF212, LOC105374344	GRCh38.p7	4:1113466	ACCCAGTTGGCCATG[C/G]CAGGCGGGCGACCGC	285498
rs759688718	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1106710	ACCAGCCTCCAGCCC[A/G]ACCGTGTACAGGGCT	285498
rs759704137	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1091033	CACAGGGGAGGCTTA[A/G]TGGGCATGATAGGAA	285498
rs759733104	in-del	-/CAAA			intron-variant	RNF212	GRCh38.p7	4:1063694	AGTGAGACTCAGTCT[-/CAAA]AAAAAAAAAAAAAAG	285498
rs759774428	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1064568	CAGCCTTCTCACTCT[C/G]TCTTCATACGGCCTC	285498
rs759803450	in-del	-/CT			intron-variant	RNF212	GRCh38.p7	4:1078162	TGCCAATGAGCCACA[-/CT]GTGTCGCACAACCCG	285498
rs759858888	snp	C/G	4.95176e-05	0.00497558	intron-variant	RNF212	GRCh38.p7	4:1090769	CAAGTGGCAATGAAT[C/G]AATTCCACTTACCTT	285498
rs759869773	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1075634	ATGAGATTCGGGCAG[A/G]GACAAATATCTAAAC	285498
rs759874857	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1099144	GGCAGCCATTCCTCC[A/G]CCCCGGCACTCACAT	285498
rs759971102	snp	G/T			intron-variant	RNF212	GRCh38.p7	4:1082356	GCCTGGTGGACATGC[G/T]GAGATGCACACGTAA	285498
rs760009964	snp	A/G	4.9516e-05	0.00497549	intron-variant	RNF212	GRCh38.p7	4:1081484	TGGAAGAGTGATGAC[A/G]AAAATGCCAGCGTCA	285498
rs760013106	snp	A/G	3.40327e-05	0.00412495	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1073227	GACAGCGTGTGGGGA[A/G]ATGGCCTGTGTGGGC	285498
rs760013821	snp	A/G	0.000186864	0.0096642	intron-variant, utr-variant-5-prime	RNF212	GRCh38.p7	4:1099899	AGGCGTGCTGTTGGT[A/G]ACTCGCTGTCAGACA	285498
rs760022752	snp	C/T			downstream-variant-500B, intron-variant	RNF212	GRCh38.p7	4:1071337	ATTTTCAAAATAAAT[C/T]ATTAAAAAAACTCAT	285498
rs760072313	in-del	-/A	1.65965e-05	0.00288062	frameshift-variant, utr-variant-5-prime, intron-variant, nc-transcript-variant	RNF212	GRCh38.p7	4:1108379	ACGACAAGGAGCTTT[-/A]CAAATCAAGCATTCA	285498
rs760128282	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1105966	CTGGGGACCACGAGG[C/T]GGCCAGAGGCCAGGC	285498
rs760137115	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1067438	AAAGATCTAACCATA[C/T]GTTGTCTATCAGAGG	285498
rs760140921	snp	C/T			synonymous-codon, intron-variant, downstream-variant-500B, nc-transcript-variant	RNF212	GRCh38.p7	4:1056878	GGGGATGCTGATGGG[C/T]GGCCGGGGGGGCAGC	285498
rs760146447	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1081700	ACTGAAAGTGTAAGA[A/C]GGCTCTGAATCAGTG	285498
rs760183853	snp	C/T			intron-variant, utr-variant-3-prime	RNF212	GRCh38.p7	4:1094125	TGAAGGAGAGTGCCA[C/T]GCAGGGGTCCATCCT	285498
rs760249642	snp	C/T	0.000183234	0.00956993	intron-variant, missense, downstream-variant-500B	RNF212	GRCh38.p7	4:1093998	AGACGGCAACAGCCT[C/T]GGGAAAGCCTGAGAT	285498
rs760312718	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1079503	CACCCCTCTCACCCA[C/T]GGGACCAGCACACGA	285498
rs760315903	snp	C/T	1.64808e-05	0.00287057	intron-variant	RNF212	GRCh38.p7	4:1096760	CCACACCCCTCACAG[C/T]TCACCTGGGAGGTTT	285498
rs760323061	in-del	-/G	1.66685e-05	0.00288686	intron-variant	RNF212	GRCh38.p7	4:1085884	GCACTCACGGGGGGT[-/G]GGGCGCCTTACCTTT	285498
rs760368762	in-del	-/G			intron-variant	RNF212	GRCh38.p7	4:1060113	AAAAAAAAAAAAAAA[-/G]GAAAAAAGAAATTGT	285498
rs760474654	snp	A/G	1.65581e-05	0.00287728	missense, intron-variant, nc-transcript-variant	RNF212	GRCh38.p7	4:1079662	CTAATCGGAGAAGGA[A/G]AGAGATCAACTTCCA	285498
rs760481390	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1059439	GCAGAGACTGCCCTC[C/G]TAGGGACAGCCAGTT	285498
rs760498702	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1085191	AAGGCATTGCTGAGC[A/G]TAATATGTGCCACAT	285498
rs760525729	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1074454	TCTGCCCCCGGCACA[A/G]CCACCCCACAGATCC	285498
rs760554093	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1092777	TCACGCGTGCTTTGC[C/G]CGCATCCTGCGAACT	285498
rs760557659	snp	C/T	0.000106572	0.00729896	utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant	RNF212, LOC105374344	GRCh38.p7	4:1113509	GGGCCCACGCGAAGC[C/T]CACGCAAGGTTGGGA	285498
rs760571384	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1069095	GCATGCCTATAGTCC[C/T]AGCTACTTGGGAGAC	285498
rs760575344	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1060583	CATCTTCCAGCGCAG[C/T]GGTCTCCGTTCAGGG	285498
rs760580889	snp	C/T	4.94858e-05	0.00497398	missense, intron-variant, nc-transcript-variant	RNF212	GRCh38.p7	4:1081456	GTGGCAGCAGGCATC[C/T]GTGTGGTTTTGCTGG	285498
rs760651257	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1082452	CTGTCTCCTGGCACC[A/G]AGTGCCCGTCTATGC	285498
rs760655380	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1105043	GCCTGCTGGGGTTCC[C/G]ATCAAGTGAAGCGAG	285498
rs760677727	snp	A/G	1.64893e-05	0.0028713	missense, intron-variant, downstream-variant-500B, nc-transcript-variant	RNF212	GRCh38.p7	4:1073160	GACAAGGTCAACCAT[A/G]GGATGAAACAGAAAG	285498
rs760814682	snp	A/T			intron-variant	RNF212	GRCh38.p7	4:1077558	CTTGAGTATTCTCTA[A/T]CCTCCTCAATTACTC	285498
rs760830577	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1057624	CAGCTGCCCCAAAAA[C/T]CAAACATATTTACTA	285498
rs760833164	in-del	-/AGCAA			intron-variant	RNF212	GRCh38.p7	4:1069195	CAGCCTGGGCAACAG[-/AGCAA]GATTGTGTCTCAAAA	285498
rs760873600	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1087948	CAATTAAACCCCTTT[C/G]CTTTATAAATCACCC	285498
rs760900509	snp	C/T	0.000370714	0.0136095	intron-variant, missense	RNF212	GRCh38.p7	4:1099733	CGTGACTGAAGGCCT[C/T]TGCTGCGTCTGACGT	285498
rs760920668	snp	A/G			missense, intron-variant, nc-transcript-variant	RNF212	GRCh38.p7	4:1056921	CCCCCGAAGCTTGGA[A/G]AGTCCCCTCTTCCTG	285498
rs760922157	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1100144	TTCATCTTCTTTTGC[C/T]TGCTGCCTGTGTGGA	285498
rs760953689	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1091586	CCTTGCCATCTGCGA[C/T]GATAACACAAGCAGG	285498
rs760962679	snp	C/T	1.66255e-05	0.00288314	intron-variant	RNF212	GRCh38.p7	4:1108306	AAAAGGAAATATGAC[C/T]GTGATTAAGATGCAG	285498
rs760987139	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1065124	AAGCATCTCTTAGAG[A/G]CCCTGCTTTCAATCC	285498
rs761018193	snp	A/C	1.65828e-05	0.00287943	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1073554	CAGGGAATGCATTTT[A/C]ATCGATGCATGTATC	285498
rs761025489	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1062457	CACTTGAAAAATTTA[A/G]CCCTTCTTCATGACA	285498
rs761121444	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1065870	GGATTACAGACATCC[A/G]TGCCCGGCCTGTTTT	285498
rs761152544	snp	A/T	1.90649e-05	0.00308741	intron-variant	RNF212	GRCh38.p7	4:1081666	ATCATAAAAACTGAC[A/T]TCCCCCCAGGTCATC	285498
rs761209392	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1089355	CCTGCAGCCCCTTTG[C/T]TTTGGTCAATTTCTC	285498
rs761287097	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1097733	CACAAAACACTAGGC[A/G]ACAGCTGTCCTAGGC	285498
rs761312372	snp	C/T	1.69945e-05	0.00291496	missense, utr-variant-5-prime, intron-variant, nc-transcript-variant	RNF212	GRCh38.p7	4:1108402	AGCATTCATTCTTTT[C/T]ACCTATAAAATAAAA	285498
rs761335616	snp	G/T	1.89755e-05	0.00308016	utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant	RNF212, LOC105374344	GRCh38.p7	4:1113483	AGGCGGGCGACCGCA[G/T]CGGCGAGGCCGGGCC	285498
rs761380535	snp	G/T			intron-variant	RNF212	GRCh38.p7	4:1105995	GCCACAGGGCCTACA[G/T]GCATGGGGGACTTTG	285498
rs761392125	snp	C/G	1.65004e-05	0.00287227	intron-variant	RNF212	GRCh38.p7	4:1081400	CAGGTCCTGTGATTT[C/G]TGCAAGCAACCCACA	285498
rs761427581	snp	A/G	3.3e-05	0.00406189	intron-variant	RNF212	GRCh38.p7	4:1081475	TGGTTTTGCTGGAAG[A/G]GTGATGACGAAAATG	285498
rs761575234	snp	G/T			intron-variant	RNF212	GRCh38.p7	4:1080637	CCTCACGGGAAACCT[G/T]CCTGGATGACGCCCT	285498
rs761575632	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1107242	ATTTTTAGTAGAGAC[A/G]GGGTTTTACCATGTT	285498
rs761605082	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1080186	TAGGATTCATTTTGC[A/G]TTGGCCCCCTCCTAG	285498
rs761695250	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1060259	GCCAAGTGTGGGCCA[C/T]GGGATCTCAGACCCG	285498
rs761714470	snp	C/T	0.000151389	0.00869894	intron-variant, missense, downstream-variant-500B	RNF212	GRCh38.p7	4:1093695	GCGCACGGCCTGTGG[C/T]TCTGATGTCTGTGAT	285498
rs761716784	snp	G/T	1.65743e-05	0.00287869	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1073561	TGCATTTTAATCGAT[G/T]CATGTATCGGTCTGA	285498
rs761772960	snp	C/T			intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1073326	TTACCAGGAAGCAAA[C/T]CCAGTGACACTATTT	285498
rs761829173	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1110455	CTAGCCACTCCACCC[C/T]GAAGAATATATTCCA	285498
rs761862843	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1083093	GAGGAAAATGCAGGC[A/G]ATACCAGGTATGTAG	285498
rs761893658	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1057253	GGGGGCGTGAGAGAA[C/T]GCTGAGGCCTGCAGG	285498
rs761912609	snp	G/T	1.65732e-05	0.00287859	intron-variant	RNF212	GRCh38.p7	4:1073667	GCTATCTCAGACTAA[G/T]AATGCAACAAGAAAA	285498
rs761918705	snp	A/T			intron-variant	RNF212	GRCh38.p7	4:1109804	GGCAGCATCTCTTCC[A/T]GCCCAAGCCCAGGCT	285498
rs762023188	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1074877	AGGTACTTCCTTTCA[C/T]CTGCCTGGAGTGCTG	285498
rs762065206	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1090240	ATGGAAGGGGAGTGA[C/G]TGGCTGGCAAGCAGG	285498
rs762081954	snp	A/G	1.76727e-05	0.00297255	intron-variant	RNF212	GRCh38.p7	4:1108417	TACCTATAAAATAAA[A/G]ATAGGCTTTATTATA	285498
rs762089546	snp	C/T	5.00597e-05	0.00500273	intron-variant	RNF212	GRCh38.p7	4:1085850	GACCAATGCACATGG[C/T]AGTGGGTGCCTCGAC	285498
rs762104763	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1082599	CCTCCTAGAGCCTGC[C/T]CTGGCACTGCCCCTC	285498
rs762170052	snp	C/T	3.31653e-05	0.00407204	intron-variant	RNF212	GRCh38.p7	4:1108317	TGACTGTGATTAAGA[C/T]GCAGATACGACACAT	285498
rs762285760	snp	A/G	1.65754e-05	0.00287879	synonymous-codon, utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1072949	TCTGAACGTGTCCAG[A/G]GTGCCCTCAGCCTGC	285498
rs762309440	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1089550	TTTGGGGGACTGCTG[C/G]GAAGGTATGATTGTG	285498
rs762327387	snp	A/G			upstream-variant-2KB, intron-variant	RNF212, TMED11P, LOC105374344	GRCh38.p7	4:1115463	TTAACTCACGATTTT[A/G]AGGGGAGGGTTGTTG	285498
rs762351589	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1084186	AAACTCCCGACCTCA[A/G]GTAATCTGCCCACCT	285498
rs762413559	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1073990	TGTTAGAGAATGTGA[A/G]ATTCTGAGTAAATCA	285498
rs762483224	snp	C/T			upstream-variant-2KB, intron-variant	RNF212, LOC105374344	GRCh38.p7	4:1114339	TGGTTTTGAGAGTTT[C/T]CACCCGCTGGGACGC	285498
rs762504040	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1085498	ATATATGTACCTTTC[A/G]CAAACGGCTACGACT	285498
rs762593688	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1098740	ATAAAACAGAAGCAG[A/G]AACAGCACCCCCTCA	285498
rs762633488	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1060472	CTCGAGAGCACCGCA[C/G]CCCTGAGGTGGGAGG	285498
rs762685245	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1108226	ACTCAGATATCTTTG[C/T]TAACGGAGCAAAGTG	285498
rs762721454	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1059684	GTTGCCTCCTCATCC[A/G]TCAGCCTCACACCAG	285498
rs762788136	snp	A/C			upstream-variant-2KB, intron-variant	RNF212, TMED11P, LOC105374344	GRCh38.p7	4:1115418	CACGGTCCTATGCGG[A/C]AAAGAAGTAGGTTTA	285498
rs762898981	snp	A/T			intron-variant	RNF212	GRCh38.p7	4:1089645	CTGTGTCCCCACCCA[A/T]ATCTCATTTTGAATT	285498
rs763004686	snp	C/T	1.67781e-05	0.00289634	intron-variant	RNF212	GRCh38.p7	4:1073698	CAATGGGTAAAATTC[C/T]AATATTGCGGCTTAC	285498
rs763037854	in-del	-/TGTTTT			intron-variant	RNF212	GRCh38.p7	4:1065880	CATCCGTGCCCGGCC[-/TGTTTT]TGTTTTTAAGAGACA	285498
rs763063534	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1100484	GCGATCTCCGCTCAC[C/T]GCAACCTCCACTCCC	285498
rs763136181	snp	A/T	5.58914e-05	0.00528607	intron-variant	RNF212	GRCh38.p7	4:1108439	TTTATTATATTAGAC[A/T]GACTACTACTTTTAA	285498
rs763152049	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1110656	GAATGGTAGACACAC[C/T]ATTGCTTTTGTTTTA	285498
rs763189959	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1106987	TCACTGATAGGAAAA[C/T]ACTAAAATATAATGC	285498
rs763199429	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1074176	AACCCACAGGAACCT[A/G]TGAACCCAGAGCTGC	285498
rs763204322	snp	C/T			synonymous-codon, intron-variant, nc-transcript-variant	RNF212	GRCh38.p7	4:1081601	TGTGCTGAAAGCTGT[C/T]TGTTGTGATGATCTC	285498
rs763245281	snp	A/C/G	8.32735e-05	0.00645218	missense, synonymous-codon, intron-variant, nc-transcript-variant	RNF212	GRCh38.p7	4:1085903	CGCCTTACCTTTGTA[A/C/G]TTGTTCTATCTGCAG	285498
rs763293638	in-del	-/TC	1.64982e-05	0.00287208	frameshift-variant, intron-variant, nc-transcript-variant	RNF212	GRCh38.p7	4:1090806	ATAGAAGGCTAACAA[-/TC]TCTTCCTGTGTTTTT	285498
rs763329824	snp	C/G	1.81056e-05	0.00300873	missense, upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant	RNF212, LOC105374344	GRCh38.p7	4:1113372	TTTGCCGAGGCAGGC[C/G]TCGCAGTACACGTGC	285498
rs763332067	snp	C/T	1.66804e-05	0.00288789	intron-variant	RNF212	GRCh38.p7	4:1085862	TGGCAGTGGGTGCCT[C/T]GACTGCGCACTCACG	285498
rs763348421	snp	A/C/T	0.000148329	0.00861069	synonymous-codon, missense, intron-variant, downstream-variant-500B, nc-transcript-variant	RNF212	GRCh38.p7	4:1073147	CACAGGGGGCTTAGA[A/C/T]AAGGTCAACCATGGG	285498
rs763470021	snp	A/C	6.58968e-05	0.00573969	missense, nc-transcript-variant	RNF212	GRCh38.p7	4:1096782	GGGAGGTTTCCCTGG[A/C]GTACTTCTTACACAG	285498
rs763472041	snp	A/C			downstream-variant-500B	RNF212	GRCh38.p7	4:1055893	GTCTCCTGCAGGAGA[A/C]CCCACCCTCCTGACG	285498
rs763570512	snp	A/G	0.000313824	0.0125225	intron-variant, utr-variant-3-prime	RNF212	GRCh38.p7	4:1094033	TGGGTGATTCAGGCT[A/G]TTTCAGAAGCAAGGA	285498
rs763623798	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1105967	TGGGGACCACGAGGC[A/G]GCCAGAGGCCAGGCC	285498
rs763625428	snp	G/T			intron-variant, utr-variant-3-prime	RNF212	GRCh38.p7	4:1094131	AGAGTGCCATGCAGG[G/T]GTCCATCCTCAGTCT	285498
rs763633142	snp	A/G	1.64773e-05	0.00287026	stop-gained, nc-transcript-variant	RNF212	GRCh38.p7	4:1096767	CCTCACAGCTCACCT[A/G]GGAGGTTTCCCTGGA	285498
rs763711643	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1104999	TTCTGGAGGAGCTCT[C/G]TTGTCTGCTGTCTCC	285498
rs763792869	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1111212	TGACATCTTCTTTAC[C/G]TCCTTCAACAAATGC	285498
rs763798854	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1067114	TTTTGAGGACATGAA[C/T]CTTATTGGCTTAGGG	285498
rs763861724	snp	C/T	1.65061e-05	0.00287277	intron-variant	RNF212	GRCh38.p7	4:1081390	GAAAGACCTGCAGGT[C/T]CTGTGATTTCTGCAA	285498
rs763944790	snp	C/T	1.73486e-05	0.00294517	missense, upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant	RNF212, LOC105374344	GRCh38.p7	4:1113398	CGTGCCCGCAGTTGG[C/T]GAGGCTGAAGCACGA	285498
rs763955146	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1100643	CAAACGCCTGACCTC[A/G]GGTGATCTGCCCGCC	285498
rs763962729	snp	A/C	0.000103568	0.00719536	intron-variant, synonymous-codon	RNF212	GRCh38.p7	4:1093481	TGCGTTTGTGATGCT[A/C]ACCTCCACAGTGTAA	285498
rs763984151	snp	C/T			intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1111724	ACCTGAAATCAACAA[C/T]TCCACTCCCAGGTTA	285498
rs764078711	snp	C/T	3.31791e-05	0.00407289	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1073557	GGAATGCATTTTAAT[C/T]GATGCATGTATCGGT	285498
rs764113230	snp	A/G			utr-variant-3-prime, intron-variant	RNF212	GRCh38.p7	4:1072465	TGGACTGCTCTGGTG[A/G]AGGATGAGGATGATG	285498
rs764125145	snp	C/T			utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1072720	TTCAAAGGTCAAATA[C/T]AAAATTACAAAGCAA	285498
rs764184715	in-del	-/CAAACAAA			intron-variant	RNF212	GRCh38.p7	4:1077229	AGTGAGACTCTGTCT[-/CAAACAAA]CAAACAAACAAAAAA	285498
rs764212168	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1081773	CAGCAGTTCCCATAG[C/T]GTCCTGTGAGTCGCA	285498
rs764228656	snp	C/T	0.000241022	0.0109751	intron-variant, missense	RNF212	GRCh38.p7	4:1099748	TTGCTGCGTCTGACG[C/T]CATCATGGCAGAGGG	285498
rs764426958	snp	C/G	1.65162e-05	0.00287365	intron-variant	RNF212	GRCh38.p7	4:1081498	CGAAAATGCCAGCGT[C/G]AGTGCACACAGTGTG	285498
rs764473990	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1099541	GGATCGGTGAGAGCT[A/G]AGGCCCTCGCATCAT	285498
rs764559603	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1082649	ACTTATCCTGACAGC[C/T]TGTGTCCCGGCCCGA	285498
rs764577892	snp	C/T	1.66158e-05	0.0028823	intron-variant	RNF212	GRCh38.p7	4:1108308	AAGGAAATATGACTG[C/T]GATTAAGATGCAGAT	285498
rs764583762	in-del	-/TT			intron-variant	RNF212	GRCh38.p7	4:1091215	AGAGCCGGCACACAG[-/TT]AATGAGGCTAAGCGA	285498
rs764590982	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1061589	CCCACATGCACAGAT[C/G]ATTGGCCATGGGGAG	285498
rs764672424	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1085420	ATCCTAGCAACTCTG[C/G]ATGTTTCTTCCTAAG	285498
rs764700468	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1059641	GGTCTCTGGGGAACT[A/G]TGAGTGGAAACTCCT	285498
rs764744815	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1103053	GAATTCATAATACCC[A/C]CTGTTAAACAAGAGG	285498
rs764798903	snp	C/T	1.65012e-05	0.00287234	intron-variant	RNF212	GRCh38.p7	4:1081480	TTGCTGGAAGAGTGA[C/T]GACGAAAATGCCAGC	285498
rs764834295	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1097097	TGCCTGGCAAGGACA[C/T]GCTCCCTCCTCAAAA	285498
rs764880135	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1091600	ATGATAACACAAGCA[A/G]GAGGGAGCGGCCTTG	285498
rs764890483	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1065140	CCCTGCTTTCAATCC[C/T]TTTGAGTACTGAATT	285498
rs764904469	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1075379	AGGAAGCATGGCAAC[A/C]GCTGCTTCTGGGGAG	285498
rs764950071	snp	A/G	1.93127e-05	0.0031074	utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant	RNF212, LOC105374344	GRCh38.p7	4:1113486	CGGGCGACCGCAGCG[A/G]CGAGGCCGGGCCCAC	285498
rs764974133	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1069432	AGTGTCATTTGGACT[A/G]TCTCTCCACAAGACA	285498
rs764988324	snp	A/G	0.0017316	0.0293735	intron-variant, missense, downstream-variant-500B	RNF212	GRCh38.p7	4:1093530	ACGAGGTCACTGGGC[A/G]GAGCCTGTGACCTCC	285498
rs765014781	in-del	-/T			intron-variant	RNF212	GRCh38.p7	4:1108733	GACAAGGTCTTGTTC[-/T]GTTGCCCAGGCTGAT	285498
rs765076395	snp	A/G	1.65378e-05	0.00287552	intron-variant	RNF212	GRCh38.p7	4:1090844	ATTCTAAAATCTGAA[A/G]AGATCATAGGTTTCA	285498
rs765092668	snp	A/G	3.31945e-05	0.00407383	intron-variant	RNF212	GRCh38.p7	4:1073671	TCTCAGACTAAGAAT[A/G]CAACAAGAAAACAAT	285498
rs765243461	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1101968	TTAAAAATGAATATA[C/T]TTCTAGGTAACACAT	285498
rs765307544	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1110508	ACAAGTGGTGTCTCA[C/T]AGCAAAACGGCAGAA	285498
rs765327526	snp	C/T			intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1111928	GATGAACTACAGTTA[C/T]ATACAAATACAATGA	285498
rs765360865	snp	A/G/T			utr-variant-3-prime, intron-variant	RNF212	GRCh38.p7	4:1072539	TGTACCTTCCTTTCA[A/G/T]TTTTTCTGTGAACCT	285498
rs765375570	snp	G/T			intron-variant	RNF212	GRCh38.p7	4:1088600	GTGCATAAGTAACCA[G/T]GAGCCAGGACGGTGG	285498
rs765386079	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1099702	AGTAACGAGGATACA[C/T]AGTTAAATCTCACAG	285498
rs765394301	snp	A/G			intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1073405	TGTGACTTGTTACAC[A/G]GTCATCAGGAGCTTC	285498
rs765398110	snp	G/T			intron-variant	RNF212	GRCh38.p7	4:1066237	TCTTGCTATAGTTTT[G/T]ATTTGCATTTCTCTA	285498
rs765423719	in-del	-/T			intron-variant	RNF212	GRCh38.p7	4:1080686	GGCCCACGAGACCCC[-/T]TCTCTGCCTGAGCCT	285498
rs765521302	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1105112	AAGACTTATCTCTTA[C/G]CACTTGGAACTCAAA	285498
rs765591275	snp	A/G	1.81665e-05	0.00301378	intron-variant	RNF212	GRCh38.p7	4:1108430	AAAATAGGCTTTATT[A/G]TATTAGACTGACTAC	285498
rs765629935	snp	A/G	3.30491e-05	0.00406491	synonymous-codon, utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1072958	GTCCAGGGTGCCCTC[A/G]GCCTGCTGGAACGGA	285498
rs765637633	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1068681	ATTCCTTCTAACAGA[C/T]TGAAGTGACTGTGTG	285498
rs765712205	snp	A/G	9.88419e-05	0.00702931	missense, synonymous-codon, intron-variant, nc-transcript-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1073055	CTTCCAGAACTGAAC[A/G]CTAGGAGGAGCAGCC	285498
rs765725407	snp	C/G	1.65696e-05	0.00287828	intron-variant	RNF212	GRCh38.p7	4:1079715	ATAGTGAAAGGCTTT[C/G]AGTGAGCCCAGGACT	285498
rs765895610	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1060738	CAGATCCACTGTGCT[A/G]TGTTCTGGAGGGGAC	285498
rs765956026	in-del	-/AGAC			upstream-variant-2KB, intron-variant	RNF212, TMED11P, LOC105374344	GRCh38.p7	4:1114838	ACTTTTATTTCTGTT[-/AGAC]AGTGCTGATCTCTAC	285498
rs765998057	snp	A/T	8.25362e-05	0.00642349	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1073589	TGAGGTTACAGGACA[A/T]TTTACTTACCCATTC	285498
rs766046880	in-del	-/G			intron-variant	RNF212	GRCh38.p7	4:1105857	AGCCTGTGGCCATCT[-/G]GGAGGACATTCCAGT	285498
rs766086507	snp	A/C	0.000215424	0.0103762	intron-variant, missense, downstream-variant-500B	RNF212	GRCh38.p7	4:1093546	GAGCCTGTGACCTCC[A/C]CGGCCCATGCCGGAA	285498
rs766173131	in-del	-/TCTT			intron-variant	RNF212	GRCh38.p7	4:1058642	TATCCTACATTTTAA[-/TCTT]TCTACCTTTATGCAC	285498
rs766204422	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1068788	GTGAATGTATTTAGT[C/T]TTCATTTTAAAATGT	285498
rs766207372	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1082657	TGACAGCCTGTGTCC[C/T]GGCCCGACATACAAG	285498
rs766295926	snp	G/T			intron-variant	RNF212	GRCh38.p7	4:1065408	TTCATAAAAATACTT[G/T]GAGGAAAGCTGCATC	285498
rs766320323	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1104161	TAACACTGTTGCACA[A/G]AGCCTCCCTAAAGAA	285498
rs766334678	in-del	-/T			intron-variant	RNF212	GRCh38.p7	4:1108725	TTTTTTGAGACAAGG[-/T]CTTGTTCTGTTGCCC	285498
rs766335413	snp	C/G/T	5.29847e-05	0.00514684	missense, upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant	RNF212, LOC105374344	GRCh38.p7	4:1113383	AGGCGTCGCAGTACA[C/G/T]GTGCCCGCAGTTGGT	285498
rs766376360	snp	A/T			intron-variant	RNF212	GRCh38.p7	4:1089486	TTGCCTTGTCTCTGA[A/T]GAGATTTTGGGCTTG	285498
rs766383753	snp	C/G	1.65493e-05	0.00287652	intron-variant	RNF212	GRCh38.p7	4:1079632	GAACTCAGCAGGAGA[C/G]ATGCACTTACTTTTC	285498
rs766414209	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1079953	GCTCTCCCTGGCATT[A/C]CTCTCTTGCACCTCT	285498
rs766536622	snp	A/G	1.65075e-05	0.00287289	intron-variant	RNF212	GRCh38.p7	4:1108455	GACTACTACTTTTAA[A/G]TATGTATACATGCAG	285498
rs766555030	snp	A/C			stop-gained, intron-variant, nc-transcript-variant	RNF212	GRCh38.p7	4:1056934	GAGAGTCCCCTCTTC[A/C]TGCTCTCCCTGGTAA	285498
rs766568645	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1100485	CGATCTCCGCTCACC[A/G]CAACCTCCACTCCCC	285498
rs766639705	snp	A/G	0.000164747	0.0090745	missense, intron-variant, nc-transcript-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1073065	TGAACGCTAGGAGGA[A/G]CAGCCAGTGAGGACA	285498
rs766693545	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1069526	GGCGACCAAGGTGAA[C/T]ATCCTCCTGGAGGAA	285498
rs766706806	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1074196	CCCAGAGCTGCCAGC[A/G]CAGGTTCTGAGACTG	285498
rs766714864	snp	C/G			downstream-variant-500B, intron-variant	RNF212	GRCh38.p7	4:1071130	TTGTTTTTTTAAATA[C/G]TGTTCTTACAATTTT	285498
rs766729338	snp	A/G	1.64944e-05	0.00287175	missense, utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1072971	TCAGCCTGCTGGAAC[A/G]GAAACAAGACGGCCC	285498
rs766736601	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1081406	CTGTGATTTCTGCAA[C/G]CAACCCACACACCTG	285498
rs766745396	snp	A/T	0.000685636	0.0185026	intron-variant, utr-variant-3-prime	RNF212	GRCh38.p7	4:1094056	AGCAAGGAAGCTCCC[A/T]GAGGAGGACAGTCTT	285498
rs766798855	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1059715	TGATTAAAACAAAAC[C/T]CTGTACATTGAACAC	285498
rs766895141	snp	G/T			intron-variant	RNF212	GRCh38.p7	4:1077504	TCCCAAAGTGCTGAA[G/T]TTATAGGCGTGAGCC	285498
rs766899794	snp	C/T	0.000230605	0.0107354	missense, nc-transcript-variant	RNF212	GRCh38.p7	4:1096793	CTGGAGTACTTCTTA[C/T]ACAGACTGTCTATGC	285498
rs766968979	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1066846	TGTTGCCTGTGCTTT[A/G]GTATCATATCCAGGA	285498
rs766978043	in-del	-/C	1.65061e-05	0.00287277	frameshift-variant, intron-variant, nc-transcript-variant	RNF212	GRCh38.p7	4:1090822	TCTTCCTGTGTTTTT[-/C]CTTGAAATTCTAAAA	285498
rs766978654	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1078169	GAGCCACACTGTGTC[A/G]CACAACCCGAAGCAA	285498
rs766998073	in-del	-/AA	0.000107313	0.00732429	utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1072826	GAAAAAACACAGAGG[-/AA]AATAAATTGAAAACA	285498
rs767064426	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1080197	TTGCGTTGGCCCCCT[C/T]CTAGCCCTGCCATCC	285498
rs767064672	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1088638	GTCTCCAGGGCATGT[A/G]AGAGATCTTCACAGC	285498
rs767102525	snp	A/G	8.22538e-05	0.0064125	intron-variant, missense, downstream-variant-500B	RNF212	GRCh38.p7	4:1093786	GGGTCCTGCTGGGAT[A/G]GAGCAGGGTGAGGGG	285498
rs767166893	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1108326	TTAAGATGCAGATAC[A/G]ACACATTTCAACTTA	285498
rs767192932	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1094433	CTTGGAGTGGAGGCG[C/T]GTGCTGACTGGGAGG	285498
rs767198016	snp	A/T			upstream-variant-2KB, intron-variant	RNF212, LOC105374344	GRCh38.p7	4:1114551	TGATATTTTTGATAT[A/T]TTAGGTTAAATATAT	285498
rs767251039	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1089755	GATAGTAAGTTCTCA[C/T]GAAATCTGATGGTTT	285498
rs767361407	snp	A/T			intron-variant	RNF212	GRCh38.p7	4:1058689	AGAATATGTAAGCCA[A/T]CTGAATCATCAGCAG	285498
rs767362387	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1110099	GCCGACTCATAAAAA[C/T]CGAAAAGTTCTTACA	285498
rs767418880	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1104847	ATCTAATGGCGGCAC[A/G]GGGCAGGACAGCTAA	285498
rs767428048	snp	C/T	1.66507e-05	0.00288532	missense, intron-variant, nc-transcript-variant	RNF212	GRCh38.p7	4:1085914	TGTAGTTGTTCTATC[C/T]GCAGCACTGACTTCC	285498
rs767451517	snp	C/T			intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1057917	AAATACAAAATTAGC[C/T]GAGTGTGGTGGCACA	285498
rs767467222	snp	C/T	0.000115484	0.00759794	missense, intron-variant, nc-transcript-variant	RNF212	GRCh38.p7	4:1090792	CTTACCTTTTCTCTA[C/T]AGAAGGCTAACAATC	285498
rs767519918	snp	A/G	1.74955e-05	0.00295761	synonymous-codon, upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant	RNF212, LOC105374344	GRCh38.p7	4:1113390	GCAGTACACGTGCCC[A/G]CAGTTGGTGAGGCTG	285498
rs767528299	in-del	-/GGGATTACA			intron-variant	RNF212	GRCh38.p7	4:1107319	GCCTCCCAAAGTGCT[-/GGGATTACA]GGTGTGAGCCACTGC	285498
rs767616846	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1081021	GCCATGGGTTGGGTA[A/G]TGGGTTCAGGCCATC	285498
rs767656268	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1103434	AAAATGTGGAAAGAG[C/T]ATTACAAGAAAAAAA	285498
rs767707389	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1084260	CTGGCCCCTTTGATG[C/T]ATTTTAAGTATCTGC	285498
rs767765003	snp	C/G			downstream-variant-500B	RNF212	GRCh38.p7	4:1056015	AGCCGGCATCACAGG[C/G]CCGCTGTGAGTACTG	285498
rs767825129	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1060579	ACAACATCTTCCAGC[A/G]CAGCGGTCTCCGTTC	285498
rs767836271	snp	A/G	1.64969e-05	0.00287196	intron-variant	RNF212	GRCh38.p7	4:1096891	CTAATAAACGCTTCT[A/G]GCCCCCAGTTAAAAA	285498
rs767855729	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1088085	TTTGGAACTGGGTAA[C/T]GGGCAGAAGTTGGAA	285498
rs767922261	snp	A/C			utr-variant-3-prime, intron-variant	RNF212	GRCh38.p7	4:1072395	GAACCCTAATGTAAA[A/C]CATGGACGTTGGGTG	285498
rs768008119	snp	C/T			downstream-variant-500B, intron-variant	RNF212	GRCh38.p7	4:1071362	ACTCATCTTACAACA[C/T]ACCTCAAGATAAACT	285498
rs768062720	snp	G/T	1.68655e-05	0.00290387	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1073216	AAGATGCAGGAGACA[G/T]CGTGTGGGGAGATGG	285498
rs768117037	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1108482	GCAGACTTTACAATG[C/T]TTCTCCAAGAAATAG	285498
rs768128142	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1064361	TGTAATCTCTAGAGG[A/C]ATCACTGAAATAATA	285498
rs768155534	in-del	-/A	6.79746e-05	0.00582947	frameshift-variant, utr-variant-5-prime, intron-variant, nc-transcript-variant	RNF212	GRCh38.p7	4:1108402	GCATTCATTCTTTTT[-/A]ACCTATAAAATAAAA	285498
rs768174502	snp	G/T			intron-variant	RNF212	GRCh38.p7	4:1069234	AAAGAAATCTATGAA[G/T]CCATATTGTTATAAA	285498
rs768194394	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1087702	ATCTCAAATTGTAAT[A/C]CCATGTGTCAAGGGG	285498
rs768205702	in-del	-/TT	1.66944e-05	0.0028891	intron-variant	RNF212	GRCh38.p7	4:1085977	TAATTACACAACCTC[-/TT]GTTATCAGACAGGCT	285498
rs768206649	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1107343	GGTGTGAGCCACTGC[A/G]CCTGGCCGAGAAGAC	285498
rs768229068	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1081474	GTGGTTTTGCTGGAA[C/G]AGTGATGACGAAAAT	285498
rs768276740	snp	A/C			downstream-variant-500B	RNF212	GRCh38.p7	4:1055808	AAGCCTCTTTTCCAA[A/C]CCTGTGTGGTCCCGG	285498
rs768285109	snp	C/T	0.000185443	0.00962741	intron-variant, utr-variant-5-prime	RNF212	GRCh38.p7	4:1099824	CACAAGGTCCGACGG[C/T]GCAAGCGGACACGGG	285498
rs768310477	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1064376	AATCACTGAAATAAT[A/G]AAGCACACAGATAAA	285498
rs768350275	in-del	-/AGGAGGA	0.000483629	0.0155429	intron-variant, utr-variant-3-prime	RNF212	GRCh38.p7	4:1094058	CAAGGAAGCTCCCAG[-/AGGAGGA]CAGTCTTGGGGACCT	285498
rs768379408	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1091905	CTGGGTGCCACCCCG[C/T]GGGCTATGAAGAGGA	285498
rs768405275	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1090187	AGATGGGGGTGACAG[A/G]ACAGGGCAAGGTGAC	285498
rs768484367	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1098593	TACACACCAAACTGC[A/G]AAGGCACAAGCAGTA	285498
rs768530984	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1098468	GAGGCAGAGGCCAAG[C/G]AGAGCATCCTGGAGG	285498
rs768539437	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1079929	CGCTGGCCGGCCCGC[C/G]CTGGTTGGGCTCTCC	285498
rs768556013	snp	A/T	1.65375e-05	0.0028755	intron-variant	RNF212	GRCh38.p7	4:1081535	CAACATGCATCTCTA[A/T]TTTGTTCTCTTTCTG	285498
rs768557306	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1083027	GGGTCGGGGGCGCAG[C/T]GGTCTGGGGCGGGTC	285498
rs768615442	snp	C/G	2.19094e-05	0.00330972	utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant	RNF212, LOC105374344	GRCh38.p7	4:1113513	CCACGCGAAGCCCAC[C/G]CAAGGTTGGGACCAG	285498
rs768719031	snp	G/T	3.30912e-05	0.00406749	intron-variant	RNF212	GRCh38.p7	4:1079607	AATGCCACACGTCTG[G/T]TATACAGAGGAACTC	285498
rs768833275	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1101188	ACCCACGGGCCTAAC[A/G]ACTGGCACTCACAGT	285498
rs768917964	snp	A/G	0.000463858	0.0152221	intron-variant, missense, downstream-variant-500B	RNF212	GRCh38.p7	4:1093879	CTGGTCTGGGTGCCC[A/G]TGTTGTGCTGACCCA	285498
rs768971813	snp	C/T	6.60633e-05	0.00574694	missense, utr-variant-3-prime, nc-transcript-variant	RNF212	GRCh38.p7	4:1073647	AGATTCTCGCAGGGC[C/T]GGCTGCTATCTCAGA	285498
rs769053233	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1073920	CCTAAAACAGTGAAC[A/G]GATAAAGGGCTCTAC	285498
rs769070223	snp	C/T	3.91911e-05	0.00442651	intron-variant	RNF212	GRCh38.p7	4:1081668	CATAAAAACTGACTT[C/T]CCCCCAGGTCATCCC	285498
rs769087316	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1089512	GCTTGGACTTCTGAG[C/T]TTATGCGGGAATGAG	285498
rs769141219	snp	C/G	1.66674e-05	0.00288676	intron-variant	RNF212	GRCh38.p7	4:1085882	GCGCACTCACGGGGG[C/G]TGGGGCGCCTTACCT	285498
rs769171997	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1110402	TTTGTGCCTGTTTGG[A/G]TCGCATTTGGGTCAG	285498
rs769240908	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1098711	AACTCCACCATGCCT[C/T]GGTCTCCCTACGTAT	285498
rs769263525	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1086074	TGGAGTTGCCCTCAC[A/G]CTGCTCAGGAGTAAA	285498
rs769271629	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1063961	TGCTAAAAAGTCAAC[C/T]AAGAAAATGTATCTT	285498
rs769285848	snp	A/G	0.000120635	0.00776548	intron-variant, utr-variant-5-prime	RNF212	GRCh38.p7	4:1099874	CGGGGCTCTCCTCAC[A/G]CAGCTGTAAAGGCGT	285498
rs769377079	snp	A/C	0.000115891	0.00761132	intron-variant	RNF212	GRCh38.p7	4:1081556	TCTCTTTCTGGCATG[A/C]TTTTACTTACTTGAA	285498
rs769387732	snp	A/G			utr-variant-3-prime, intron-variant	RNF212	GRCh38.p7	4:1072124	AGAAGAGATGGGGGA[A/G]CCATAAGTGTGTATT	285498
rs769443890	snp	A/G	1.72639e-05	0.00293796	intron-variant	RNF212	GRCh38.p7	4:1081633	TACTAAATAGATGGA[A/G]AAAAGGTATTGAATT	285498
rs769513962	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1077025	ACAAGGTCAGGAGTT[C/T]GAGACCAGCCTGACC	285498
rs769551126	snp	A/G	0.000149555	0.00864611	intron-variant, synonymous-codon, downstream-variant-500B	RNF212	GRCh38.p7	4:1093913	TTCTTGGGGATCTCT[A/G]GCTGCTGCTTGGCTT	285498
rs769642054	snp	C/G	2.06862e-05	0.003216	missense, utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1072906	TTTCAAATTGGCAAA[C/G]AGGAAACACAACAGA	285498
rs769652101	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1104088	ATAAGCACTTGAGAA[A/G]AATTGTTTAAAACTA	285498
rs769712820	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1074037	TTTGTCACCTTGAAA[C/T]CCAGATGCTGATGGA	285498
rs769726595	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1098245	GGCTCCCCAAATCCC[A/C]CTGAAATGATAGTAA	285498
rs769865800	in-del	-/A			intron-variant	RNF212	GRCh38.p7	4:1102871	AAAGGCCGGGCACGG[-/A]TGGCTCACACCTGTA	285498
rs769945088	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1084916	AGAGGCAATCAGAAC[C/T]TCGTGTCAGGAGCAA	285498
rs770019859	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1069016	AGTTTGAGACCATCA[C/T]GGGCAACATGGCGAA	285498
rs770040147	snp	A/G	1.65658e-05	0.00287795	intron-variant	RNF212	GRCh38.p7	4:1079710	AACACATAGTGAAAG[A/G]CTTTGAGTGAGCCCA	285498
rs770048052	snp	G/T	1.66549e-05	0.00288568	missense, intron-variant, nc-transcript-variant	RNF212	GRCh38.p7	4:1085900	GGGCGCCTTACCTTT[G/T]TAGTTGTTCTATCTG	285498
rs770052826	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1107999	TTTAAACTTACTTTA[C/T]GAACAACACTCTTAA	285498
rs770280501	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1099957	TCTTATCATCATGGA[A/G]GCTGATGCAGCCACT	285498
rs770293388	snp	A/C	1.64751e-05	0.00287007	missense, intron-variant, downstream-variant-500B, nc-transcript-variant	RNF212	GRCh38.p7	4:1073134	CACACTCTCCGGGCA[A/C]AGGGGGCTTAGACAA	285498
rs770353263	in-del	-/TT			intron-variant, utr-variant-3-prime	RNF212	GRCh38.p7	4:1093383	ATATTGTAACAAATG[-/TT]CCAATATTTATGTTA	285498
rs770448181	in-del	-/AG			intron-variant	RNF212	GRCh38.p7	4:1064598	CTTTTGTGTGTGTGC[-/AG]AGTTAGTAAGCAAGC	285498
rs770499451	snp	G/T			intron-variant	RNF212	GRCh38.p7	4:1099372	CCTGATAGAAGCACA[G/T]AGATTCGGGAGGCAG	285498
rs770538866	snp	A/T			intron-variant	RNF212	GRCh38.p7	4:1062275	AGCGTATAAGAAAGA[A/T]CATACACCACGACCA	285498
rs770542288	snp	A/G	1.72451e-05	0.00293637	missense, utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1072926	AACACAACAGACACA[A/G]CGGGTGTTCTGAACG	285498
rs770623112	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1100430	TTTTTTTTTTTGAGA[C/T]GGAGTCTTACCCTGT	285498
rs770626648	snp	A/T			intron-variant	RNF212	GRCh38.p7	4:1061226	TGCTCCACCTCCCCC[A/T]ACCCCACTCTACCCA	285498
rs770712334	snp	A/G			intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1112085	TGGCTGCACATGCCT[A/G]TAGCCCCGCTACCCT	285498
rs770760451	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1078743	ACCAGCAGAGGATCA[A/G]CGCAGGATCAACACA	285498
rs770820221	snp	C/G	4.94654e-05	0.00497295	intron-variant	RNF212	GRCh38.p7	4:1096746	ATCACGGAACCAAGC[C/G]ACACCCCTCACAGCT	285498
rs770838976	in-del	-/TGAG	1.65681e-05	0.00287815	intron-variant	RNF212	GRCh38.p7	4:1079714	CATAGTGAAAGGCTT[-/TGAG]TGAGCCCAGGACTTA	285498
rs770855820	in-del	-/A			upstream-variant-2KB, intron-variant	RNF212, TMED11P, LOC105374344	GRCh38.p7	4:1114871	CAAGTTTAAAATAGC[-/A]AAGACCAGCAACGTG	285498
rs770879474	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1064564	ACAGCAGCCTTCTCA[C/T]TCTGTCTTCATACGG	285498
rs770893646	in-del	-/G			intron-variant	RNF212	GRCh38.p7	4:1088556	AAAAACCCATTTTCT[-/G]AGGGGAAATTCAAGC	285498
rs770923757	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1085395	ATGCTTTAAGTCCCC[A/G]TTTTGGTTAATCCTA	285498
rs770938466	snp	C/T			missense, nc-transcript-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1058330	CACTACCTGAGAGGC[C/T]TTCCCATGCTCCTCT	285498
rs770942172	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1102499	GTTCAAGAGTCCACA[A/G]TACTAATAAAAATCA	285498
rs770978020	snp	C/T			intron-variant, missense	RNF212	GRCh38.p7	4:1094301	CCTGGCAGCTTTCCC[C/T]CAGACTGGTGGACTG	285498
rs770989872	snp	C/T	2.05248e-05	0.00320343	utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant	RNF212, LOC105374344	GRCh38.p7	4:1113499	CGGCGAGGCCGGGCC[C/T]ACGCGAAGCCCACGC	285498
rs771153004	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1082188	AGAAAAACAGGCCAG[C/T]AAGAGAAATATGGAC	285498
rs771166078	snp	A/T			intron-variant	RNF212	GRCh38.p7	4:1111523	TTTGTCTAGCAGTGA[A/T]ACCCTGTCCAGTTCT	285498
rs771169517	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1092260	GAGACGAGGTCAGTC[C/T]GTGGCTGATCCTGAT	285498
rs771186699	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1075562	CAGGGATCTGCCCCC[A/G]TAACCCAAACTTCTG	285498
rs771206713	snp	A/C/T	3.52567e-05	0.00419849	missense, upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant	RNF212, LOC105374344	GRCh38.p7	4:1113458	TACAGAACACCCAGT[A/C/T]GGCCATGCCAGGCGG	285498
rs771405644	snp	A/G	1.66504e-05	0.0028853	intron-variant	RNF212	GRCh38.p7	4:1090880	TGACACAGATCCACG[A/G]TCTCTGTGGCTGGAG	285498
rs771446396	snp	C/G			utr-variant-3-prime, intron-variant	RNF212	GRCh38.p7	4:1072189	ACTGTACAATTCCAA[C/G]TCCAGGAGAGTCTGA	285498
rs771450829	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1067287	AGTTAAGGAGATACC[A/G]ATAAACTAAAAATCC	285498
rs771462794	in-del	-/AGATACG	1.65784e-05	0.00287905	intron-variant	RNF212	GRCh38.p7	4:1108320	CTGTGATTAAGATGC[-/AGATACG]ACACATTTCAACTTA	285498
rs771601840	snp	A/G	3.39064e-05	0.00411728	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1073223	AGGAGACAGCGTGTG[A/G]GGAGATGGCCTGTGT	285498
rs771606426	in-del	-/T	1.65861e-05	0.00287972	frameshift-variant, intron-variant, nc-transcript-variant	RNF212	GRCh38.p7	4:1081579	TACTTGAAACTGAAC[-/T]TTTTATTGTGCTGAA	285498
rs771637487	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1062427	CAATAATCATCTCAA[A/G]AGAGAAAGAGAAAGC	285498
rs771685034	in-del	-/TG			intron-variant	RNF212	GRCh38.p7	4:1067047	ATTTCTCAAAAAAAC[-/TG]TGTCCTTTCCCCCAC	285498
rs771821414	snp	G/T			intron-variant	RNF212	GRCh38.p7	4:1069065	ATACAAAAACAATTA[G/T]CTGGGTGTGGTGGTG	285498
rs771825098	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1059319	CTGAGAAGGCTCCAA[A/G]GAACAGCTAAGAGCA	285498
rs771844895	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1100034	ATTTACTGTCTTGAA[A/G]CACACAGATTGTACT	285498
rs771911591	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1080299	CTCCAATTAGTCCAG[A/C]CTGGCTGGAGTGAAT	285498
rs771922216	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1106573	GAAAAGCGGTACTCA[A/G]AATGATACAGAATAG	285498
rs771937607	snp	C/T	1.80703e-05	0.0030058	utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant	RNF212, LOC105374344	GRCh38.p7	4:1113467	CCCAGTTGGCCATGC[C/T]AGGCGGGCGACCGCA	285498
rs771966630	snp	G/T			intron-variant	RNF212	GRCh38.p7	4:1081688	CAGGTCATCCCAACT[G/T]AAAGTGTAAGAAGGC	285498
rs771977056	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1092277	TGGCTGATCCTGATT[C/T]GGCAGGGCAGGTGTT	285498
rs771992377	snp	C/G	1.64776e-05	0.00287028	intron-variant	RNF212	GRCh38.p7	4:1096848	CGTCGGTCTGAAAGA[C/G]AAAGAAATGACTCTA	285498
rs772004272	in-del	-/A			intron-variant	RNF212	GRCh38.p7	4:1101776	CTTCCTTCTCAGCGC[-/A]AAAAATATCTGTACA	285498
rs772029243	in-del	-/AACAA			intron-variant	RNF212	GRCh38.p7	4:1103621	GCAACTCACCACATT[-/AACAA]AACAAAATAAATGAG	285498
rs772066692	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1103921	ATAAGGAATAGAAAG[A/G]GAGATCTAAAGCGTC	285498
rs772089540	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1077830	TGGGCCAGTTGCCTA[C/G]GGAGGAGGTGCACCC	285498
rs772186429	snp	C/T	1.64953e-05	0.00287182	synonymous-codon, intron-variant, nc-transcript-variant	RNF212	GRCh38.p7	4:1081442	GGCTGATGAGTGAGG[C/T]GGCAGCAGGCATCCG	285498
rs772237356	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1066338	CTGCCCTCCGCTTTT[C/G]TTTTTTCTGAGACAG	285498
rs772244466	snp	C/T	1.64814e-05	0.00287061	intron-variant	RNF212	GRCh38.p7	4:1096870	ATGACTCTACATTTA[C/T]TGTGTCTAATAAACG	285498
rs772266992	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1110261	AGACCTGAATAGGCA[C/T]AGGAAAAAATGCAAA	285498
rs772274005	snp	C/T	0.000327194	0.0127863	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1073236	TGGGGAGATGGCCTG[C/T]GTGGGCTGAGGTGGA	285498
rs772342470	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1074975	CCCCTTGACATCACC[A/G]TCCCTTCGAACTACA	285498
rs772345473	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1076736	TTGGTTTTAGACACT[C/T]TCCTTGAAATTTGCA	285498
rs772363952	snp	C/T	0.000103761	0.00720208	intron-variant, missense	RNF212	GRCh38.p7	4:1093468	GAAAACTCCACCCTG[C/T]GTTTGTGATGCTCAC	285498
rs772476290	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1082939	TCGTGGGAGCAAGAG[A/G]ATGATGACAAAAACA	285498
rs772506025	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1099467	ACTGTATGGTGGGGC[C/T]TCCTGCAGTGAGAGC	285498
rs772588607	snp	C/T	0.00020022	0.0100035	intron-variant, utr-variant-5-prime	RNF212	GRCh38.p7	4:1099926	GACACAGGAAAGGGG[C/T]GCTGCAAAAGAGGGC	285498
rs772593862	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1109603	AGCAACACTGCTGGG[A/C]AATCCTGCTTTTCCT	285498
rs772718590	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1057582	CACTGCCTGCCCCGG[A/C]CTTCTCAATACAGAG	285498
rs772725064	snp	A/G	4.96841e-05	0.00498393	intron-variant	RNF212	GRCh38.p7	4:1081561	TTCTGGCATGATTTT[A/G]CTTACTTGAAACTGA	285498
rs772748298	snp	C/G	0.000186064	0.00964351	intron-variant, utr-variant-5-prime	RNF212	GRCh38.p7	4:1099885	TCACGCAGCTGTAAA[C/G]GCGTGCTGTTGGTGA	285498
rs772758546	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1098668	CCAGCTCTGCACACC[C/T]TTGACCTGCAACCCT	285498
rs772842409	snp	A/G	0.000153315	0.0087541	intron-variant, missense, downstream-variant-500B	RNF212	GRCh38.p7	4:1093714	GATGTCTGTGATAAC[A/G]GACATGTTTTATGAA	285498
rs772857915	snp	A/T			intron-variant	RNF212	GRCh38.p7	4:1097895	CATGGTGAAACCCCA[A/T]CTCTATCAAAAATAC	285498
rs772934216	snp	C/G	1.7443e-05	0.00295317	missense, utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1072924	GAAACACAACAGACA[C/G]AGCGGGTGTTCTGAA	285498
rs772942622	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1106982	AAGGCTCACTGATAG[A/G]AAAATACTAAAATAT	285498
rs772973484	snp	A/G			synonymous-codon, intron-variant, nc-transcript-variant	RNF212	GRCh38.p7	4:1081577	CTTACTTGAAACTGA[A/G]CTTTTTATTGTGCTG	285498
rs773071691	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1065343	CATTTATTTAAAGGA[A/G]AACATCTGCAGACCA	285498
rs773125545	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1104107	TGTTTAAAACTACAA[C/T]AGTAGCAGTCCAAAT	285498
rs773132876	snp	G/T			upstream-variant-2KB, nc-transcript-variant, intron-variant	RNF212, TMED11P, LOC105374344	GRCh38.p7	4:1115307	TCAGGTACTTCATTT[G/T]GAAAATTCCGACTGA	285498
rs773145525	snp	C/G	1.66527e-05	0.00288549	intron-variant	RNF212	GRCh38.p7	4:1073678	CTAAGAATGCAACAA[C/G]AAAACAATGGGTAAA	285498
rs773183887	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1081699	AACTGAAAGTGTAAG[A/G]AGGCTCTGAATCAGT	285498
rs773214671	snp	C/T	0.000147634	0.00859042	intron-variant, missense, downstream-variant-500B	RNF212	GRCh38.p7	4:1093932	GCTGCTTGGCTTCCA[C/T]GGGTCGAGCCTCTGG	285498
rs773280409	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1100483	TGCGATCTCCGCTCA[C/G]CGCAACCTCCACTCC	285498
rs773285572	in-del	-/A			intron-variant	RNF212	GRCh38.p7	4:1102990	TACTAAAAAAATACA[-/A]AAAAAAAAAAAATCA	285498
rs773344276	snp	G/T	1.65466e-05	0.00287628	intron-variant	RNF212	GRCh38.p7	4:1079621	GGTATACAGAGGAAC[G/T]CAGCAGGAGAGATGC	285498
rs773361332	snp	A/G	1.84289e-05	0.00303548	intron-variant	RNF212	GRCh38.p7	4:1108436	GGCTTTATTATATTA[A/G]ACTGACTACTACTTT	285498
rs773466330	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1096957	TCAAGTGGCCAGCAC[A/G]TTGTGAATGGCCTCT	285498
rs773517622	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1076867	TACTTTCTATGGTTG[C/T]TTTTGCAATTCCATG	285498
rs773553181	snp	G/T	1.8255e-05	0.00302112	missense, upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant	RNF212, LOC105374344	GRCh38.p7	4:1113370	CCTTTGCCGAGGCAG[G/T]CGTCGCAGTACACGT	285498
rs773556614	in-del	-/A	8.30255e-05	0.0064425	intron-variant	RNF212	GRCh38.p7	4:1090745	TTAAATCTAAAGGTC[-/A]AAAAAATTCAAGTGG	285498
rs773576734	snp	A/G	1.64751e-05	0.00287007	synonymous-codon, missense, intron-variant, nc-transcript-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1073059	CAGAACTGAACGCTA[A/G]GAGGAGCAGCCAGTG	285498
rs773596596	snp	A/G	1.6477e-05	0.00287024	missense, synonymous-codon, intron-variant, downstream-variant-500B, nc-transcript-variant	RNF212	GRCh38.p7	4:1073139	TCTCCGGGCACAGGG[A/G]GCTTAGACAAGGTCA	285498
rs773601912	snp	A/G			downstream-variant-500B	RNF212	GRCh38.p7	4:1055866	CTCTCTGGGAGCCAC[A/G]TGCACGGGGGCGTCT	285498
rs773616672	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1083122	AGAGAGTGGGATTGG[A/C]CTGTGCAACCTCACC	285498
rs773661727	snp	G/T	3.30453e-05	0.00406467	intron-variant	RNF212	GRCh38.p7	4:1090757	GTCAAAAAAATTCAA[G/T]TGGCAATGAATCAAT	285498
rs773669548	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1102415	TCTCATGAATACTGT[A/G]TTTTTGATCTGCATC	285498
rs773704901	snp	C/T			upstream-variant-2KB, intron-variant	RNF212, TMED11P, LOC105374344	GRCh38.p7	4:1115462	CTTAACTCACGATTT[C/T]GAGGGGAGGGTTGTT	285498
rs773727944	snp	A/G			upstream-variant-2KB, intron-variant	RNF212, TMED11P, LOC105374344	GRCh38.p7	4:1115533	TACACCAACGTATCC[A/G]TGCAGTCTGCTTTTC	285498
rs773737947	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1088586	CTGGCTGCAGAAATG[C/T]GCATAAGTAACCAGG	285498
rs773747595	snp	A/C	1.75041e-05	0.00295833	missense, upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant	RNF212, LOC105374344	GRCh38.p7	4:1113454	CGATTACAGAACACC[A/C]AGTTGGCCATGCCAG	285498
rs773749734	snp	C/T	0.000516181	0.0160569	synonymous-codon, intron-variant, nc-transcript-variant	RNF212	GRCh38.p7	4:1085901	GGCGCCTTACCTTTG[C/T]AGTTGTTCTATCTGC	285498
rs773775938	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1065861	AAAGTGCTGGGATTA[A/C]AGACATCCGTGCCCG	285498
rs773806144	snp	C/T	5.14831e-05	0.00507335	missense, utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1072927	ACACAACAGACACAG[C/T]GGGTGTTCTGAACGT	285498
rs773894178	snp	A/G	3.61494e-05	0.00425128	intron-variant	RNF212	GRCh38.p7	4:1081654	GTATTGAATTAAATC[A/G]TAAAAACTGACTTCC	285498
rs773964644	snp	C/T	1.65518e-05	0.00287674	missense, intron-variant, synonymous-codon, nc-transcript-variant	RNF212	GRCh38.p7	4:1079645	GAGATGCACTTACTT[C/T]TCTAATCGGAGAAGG	285498
rs774062889	in-del	-/ACAC			intron-variant	RNF212	GRCh38.p7	4:1106262	CTTACACACACACAC[-/ACAC]ACACACACACACACA	285498
rs774105052	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1098830	TGGCCCATGTGAGTG[A/C]GCAGGGAGCGGGAAC	285498
rs774106945	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1099388	AGATTCGGGAGGCAG[C/T]GAGGAGCAGGGAAGA	285498
rs774157268	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1068335	CTCCAATGCCTCTGT[C/G]TCCTTTGTCCTTCTA	285498
rs774215528	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1057802	GGGCATGGTGGCTCA[C/T]GCCTGTAATCCCAGC	285498
rs774227876	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1081628	TCTCATACTAAATAG[A/C]TGGAGAAAAGGTATT	285498
rs774278600	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1104804	TAGAAAGACAATGAA[C/T]GTGTCTGCATCCTCG	285498
rs774325832	snp	A/G	0.000145465	0.0085271	intron-variant, missense, downstream-variant-500B	RNF212	GRCh38.p7	4:1093947	TGGGTCGAGCCTCTG[A/G]GCACCTCCTTGGAGG	285498
rs774353599	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1074498	CCCTTCCAGTACACC[A/G]TGGAAGCCCCTCTGT	285498
rs774362214	snp	A/C	4.97319e-05	0.00498633	intron-variant	RNF212	GRCh38.p7	4:1079733	TGAGCCCAGGACTTA[A/C]CTCTAACAACGTCAG	285498
rs774405194	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1089134	CAACAGCTTGCACTG[C/T]GCACCTAGAAAAGCT	285498
rs774425699	snp	A/G			downstream-variant-500B	RNF212	GRCh38.p7	4:1055983	ATCTCTGGACCTGAC[A/G]GAGATTCACCCGCTG	285498
rs774447091	snp	A/C	1.65075e-05	0.00287289	intron-variant	RNF212	GRCh38.p7	4:1090767	TTCAAGTGGCAATGA[A/C]TCAATTCCACTTACC	285498
rs774541714	in-del	-/A			upstream-variant-2KB, intron-variant	RNF212, LOC105374344	GRCh38.p7	4:1114630	GACTAGAAAACTTAG[-/A]ATTACGTATGGGCTG	285498
rs774711034	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1082253	CTGGACTGATCTCCA[C/T]GATGGCCAGTAGCAG	285498
rs774773612	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1074309	GCCCCTTCCTGGGCT[C/T]GCTCCTCTGGCTCTC	285498
rs774790406	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1092227	CTGGTCTGGCTGTTC[C/T]TAGAGAAAGGCCTTG	285498
rs774800811	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1081667	TCATAAAAACTGACT[C/T]CCCCCCAGGTCATCC	285498
rs774830888	snp	C/G	1.69971e-05	0.00291518	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1073225	GAGACAGCGTGTGGG[C/G]AGATGGCCTGTGTGG	285498
rs774877278	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1079457	CAGGCAGAACAGGAG[C/T]GTTCTCATGACCCAG	285498
rs774889937	in-del	-/ACG	0.000165475	0.00909452	cds-indel, intron-variant, nc-transcript-variant	RNF212	GRCh38.p7	4:1108364	TGAAAGCAAAACTGT[-/ACG]ACAAGGAGCTTTACA	285498
rs774918798	snp	A/G	1.64838e-05	0.00287083	missense, intron-variant, downstream-variant-500B, nc-transcript-variant	RNF212	GRCh38.p7	4:1073151	GGGGGCTTAGACAAG[A/G]TCAACCATGGGATGA	285498
rs774978445	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1104892	CACACCAAGGGAGGA[A/G]GAAGAACACAGGTGC	285498
rs775009326	in-del	-/A	1.7789e-05	0.00298231	intron-variant	RNF212	GRCh38.p7	4:1081649	AAAAGGTATTGAATT[-/A]AATCATAAAAACTGA	285498
rs775048273	snp	A/T	1.64743e-05	0.00287	synonymous-codon, stop-gained, intron-variant, nc-transcript-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1073042	GAGTTCCCCGTGCCT[A/T]CCAGAACTGAACGCT	285498
rs775092947	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1062512	CAACCCTATAAAGGG[C/T]GCCTCCAGGAAACCC	285498
rs775187430	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1083940	AGTAATTCCACATTT[C/T]GTGCATTTTTTTTTT	285498
rs775268769	snp	A/G	1.64811e-05	0.00287059	intron-variant	RNF212	GRCh38.p7	4:1096758	AGCCACACCCCTCAC[A/G]GCTCACCTGGGAGGT	285498
rs775359876	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1084199	CAGGTAATCTGCCCA[C/T]CTTGGCCTCCCAAAG	285498
rs775377075	snp	C/T	1.64961e-05	0.00287189	synonymous-codon, intron-variant, nc-transcript-variant	RNF212	GRCh38.p7	4:1081454	AGGTGGCAGCAGGCA[C/T]CCGTGTGGTTTTGCT	285498
rs775385706	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1058690	GAATATGTAAGCCAT[C/G]TGAATCATCAGCAGC	285498
rs775395271	snp	G/T	0.000510856	0.0159739	intron-variant, missense	RNF212	GRCh38.p7	4:1093473	CTCCACCCTGCGTTT[G/T]TGATGCTCACCTCCA	285498
rs775402426	snp	A/C/T	9.15401e-05	0.00676485	utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant	RNF212, LOC105374344	GRCh38.p7	4:1113471	GTTGGCCATGCCAGG[A/C/T]GGGCGACCGCAGCGG	285498
rs775453290	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1105956	AGCTGGCTGCCTGGG[A/G]ACCACGAGGCGGCCA	285498
rs775469158	snp	C/T	3.30202e-05	0.00406313	intron-variant	RNF212	GRCh38.p7	4:1081381	GCAGAATCGGAAAGA[C/T]CTGCAGGTCCTGTGA	285498
rs775469340	in-del	-/CACT			intron-variant	RNF212	GRCh38.p7	4:1074325	GCTCCTCTGGCTCTC[-/CACT]CACTGCTGGCATCTC	285498
rs775476401	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1069069	AAAAACAATTAGCTG[C/G]GTGTGGTGGTGCATG	285498
rs775568308	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1080416	TTCCAGTTCTCCACC[C/T]GCTCCCAGTGTCTCA	285498
rs775576295	in-del	-/GCCCACGCGAA	0.000100857	0.0071006	utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant	RNF212, LOC105374344	GRCh38.p7	4:1113495	CAGCGGCGAGGCCGG[-/GCCCACGCGAA]GCCCACGCGAAGCCC	285498
rs775591264	snp	C/T	1.6607e-05	0.00288153	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1073548	ACCTTTCAGGGAATG[C/T]ATTTTAATCGATGCA	285498
rs775644407	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1076908	GTAGCTGTGGACTGT[C/T]TGGTCTGCAAAGTCC	285498
rs775650198	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1092317	AGGACTGGGCTGCAG[C/G]GAAAGTCTCCAAGGG	285498
rs775737942	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1103934	AGAGAGATCTAAAGC[A/G]TCCTTATTCAAAGAT	285498
rs775740461	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1061519	GTGCAGGGGGATCCA[A/G]CGCGGCCACAGAAGT	285498
rs775825787	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1096664	TCTCGGGATAGTGCA[C/T]CTGGCTCATCACAGA	285498
rs775834973	snp	G/T			intron-variant	RNF212	GRCh38.p7	4:1065102	ACTGCTACGATCTTG[G/T]GTATACAAGCATCTC	285498
rs775848912	snp	G/T	1.68957e-05	0.00290647	missense, utr-variant-5-prime, intron-variant, nc-transcript-variant	RNF212	GRCh38.p7	4:1108398	ATCAAGCATTCATTC[G/T]TTTTACCTATAAAAT	285498
rs775858739	snp	C/T	0.000243398	0.011029	intron-variant	RNF212	GRCh38.p7	4:1099963	CATCATGGAGGCTGA[C/T]GCAGCCACTGCCGCT	285498
rs775909679	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1110272	GGCATAGGAAAAAAT[A/G]CAAACAGCCAATAAA	285498
rs775949733	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1083010	TGAGGCCGGGCAAGA[C/T]GGGGTCGGGGGCGCA	285498
rs775966266	snp	C/T	1.65913e-05	0.00288017	missense, intron-variant, nc-transcript-variant	RNF212	GRCh38.p7	4:1081581	CTTGAAACTGAACTT[C/T]TTATTGTGCTGAAAG	285498
rs776037901	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1082428	CATGACTGCACATGA[C/G]GGGTGGGGCTGTCTC	285498
rs776057140	snp	G/T	1.64746e-05	0.00287002	missense, nc-transcript-variant	RNF212	GRCh38.p7	4:1096781	TGGGAGGTTTCCCTG[G/T]AGTACTTCTTACACA	285498
rs776103045	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1106714	GCCTCCAGCCCGACC[A/G]TGTACAGGGCTTAGT	285498
rs776165006	snp	C/T	1.64841e-05	0.00287085	intron-variant	RNF212	GRCh38.p7	4:1096880	ATTTATTGTGTCTAA[C/T]AAACGCTTCTGGCCC	285498
rs776198472	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1105972	ACCACGAGGCGGCCA[C/G]AGGCCAGGCCACAGG	285498
rs776203122	in-del	-/G	1.64893e-05	0.0028713	intron-variant	RNF212	GRCh38.p7	4:1096744	TCATCACGGAACCAA[-/G]CCACACCCCTCACAG	285498
rs776249392	snp	A/G			downstream-variant-500B	RNF212	GRCh38.p7	4:1055829	GTGGTCCCGGCTGGC[A/G]GGAGAGACCTGGGCT	285498
rs776293197	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1069356	AATGGAAAAACTGCT[A/G]TGAGGCAGTCATTAG	285498
rs776329566	in-del	-/G			intron-variant	RNF212	GRCh38.p7	4:1059407	CACGGTTTGGCATCT[-/G]GAGGCTTGTGGACCC	285498
rs776357046	snp	C/T	1.65455e-05	0.00287619	intron-variant	RNF212	GRCh38.p7	4:1081547	CTATTTTGTTCTCTT[C/T]CTGGCATGATTTTAC	285498
rs776389649	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1090210	AAGGTGACAAGACAG[A/G]GTGGGGGTGACAGGA	285498
rs776499134	snp	A/T			intron-variant	RNF212	GRCh38.p7	4:1059569	CACTCACCCTGCCTG[A/T]TCCTCCCATGAGAAC	285498
rs776501793	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1075816	GCTGGGACTACAGGT[C/G]TGCACCACCATGCCC	285498
rs776537932	snp	A/C	0.000102822	0.00716943	intron-variant, missense	RNF212	GRCh38.p7	4:1093484	GTTTGTGATGCTCAC[A/C]TCCACAGTGTAACTG	285498
rs776594319	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1085305	ACAGATGCAATACGG[C/T]AAAAGCACGGATGAG	285498
rs776608679	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1060237	CTGGCAAGCAGTGCT[C/T]AAGAGAGCCAAGTGT	285498
rs776644357	snp	A/G	3.30316e-05	0.00406383	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	RNF212	GRCh38.p7	4:1073648	GATTCTCGCAGGGCC[A/G]GCTGCTATCTCAGAC	285498
rs776725009	in-del	-/T			intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1112273	AGAAAGCGGCTTTGC[-/T]TGTAGGGCTGGTTGT	285498
rs776734207	snp	A/G	0.000151343	0.00869763	intron-variant, missense, downstream-variant-500B	RNF212	GRCh38.p7	4:1093686	CACCCTGGAGCGCAC[A/G]GCCTGTGGCTCTGAT	285498
rs776811636	in-del	-/T			intron-variant	RNF212	GRCh38.p7	4:1089351	GGGGCCTGCAGCCCC[-/T]TTGTTTTGGTCAATT	285498
rs776843060	snp	A/G	1.65466e-05	0.00287628	intron-variant	RNF212	GRCh38.p7	4:1079614	CACGTCTGGTATACA[A/G]AGGAACTCAGCAGGA	285498
rs776968322	snp	A/T			intron-variant	RNF212	GRCh38.p7	4:1073974	CAAAATTTGCAGCTG[A/T]TGTTAGAGAATGTGA	285498
rs777090342	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1062515	CCCTATAAAGGGCGC[C/T]TCCAGGAAACCCTCA	285498
rs777099523	snp	A/G	2.13993e-05	0.00327096	intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1113348	GCCTGCGTTCGGGAA[A/G]CCCTGACCTTTGCCG	285498
rs777106494	snp	A/G	5.24214e-05	0.00511937	intron-variant	RNF212	GRCh38.p7	4:1108414	TTTTACCTATAAAAT[A/G]AAAATAGGCTTTATT	285498
rs777137480	snp	C/G	4.97839e-05	0.00498893	missense, utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1072948	TTCTGAACGTGTCCA[C/G]GGTGCCCTCAGCCTG	285498
rs777215071	snp	A/G	1.65649e-05	0.00287788	missense, utr-variant-5-prime, intron-variant, nc-transcript-variant	RNF212	GRCh38.p7	4:1108371	AAAACTGTACGACAA[A/G]GAGCTTTACAAATCA	285498
rs777249686	snp	C/G			intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1073289	GATTCACTTTGAAAA[C/G]GGACCAGCAATTCAA	285498
rs777328973	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1109462	GGGAGGACATCAGGT[C/T]CAAACCTGAACAAGC	285498
rs777405762	snp	A/G/T	0.000101599	0.00712674	intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1113339	CCCTCTCCAGCCTGC[A/G/T]TTCGGGAAGCCCTGA	285498
rs777525264	snp	C/T	1.66593e-05	0.00288607	missense, intron-variant, nc-transcript-variant	RNF212	GRCh38.p7	4:1085939	ACTTCCTAAGGGATT[C/T]TTCCAACCTAGAAAT	285498
rs777525654	snp	A/G			intron-variant, utr-variant-5-prime	RNF212	GRCh38.p7	4:1099838	GCGCAAGCGGACACG[A/G]GTACCCCTGTGCGGG	285498
rs777569330	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1085162	GTGACTATTCAACGC[A/G]TCTCGTAGAATCTAA	285498
rs777579306	in-del	-/AA	3.33611e-05	0.00408405	intron-variant	RNF212	GRCh38.p7	4:1073684	ATGCAACAAGAAAAC[-/AA]TGGGTAAAATTCCAA	285498
rs777605751	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1083464	CCTGGTCAACATGGT[A/G]AAGCCCCGTCTCTAC	285498
rs777607445	snp	C/G	1.64735e-05	0.00286993	missense, intron-variant, downstream-variant-500B, nc-transcript-variant	RNF212	GRCh38.p7	4:1073106	CAGAAACATGGTGAA[C/G]CTCTGGAAATGACAC	285498
rs777658717	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1078478	ACTCTCCCTGAGTTC[C/T]GGGCAGGTTTCCTCT	285498
rs777719864	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1098461	GCTCCCAGAGGCAGA[A/G]GCCAAGCAGAGCATC	285498
rs777723428	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1103990	TAGCAGAATCTACAC[A/G]TAAACCAACAGAGTT	285498
rs777781439	snp	C/G	3.29826e-05	0.00406082	intron-variant	RNF212	GRCh38.p7	4:1096741	GGCTCATCACGGAAC[C/G]AAGCCACACCCCTCA	285498
rs777807785	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1107390	GGTAAATCACAATAA[C/G]ACACATAGAATAGGT	285498
rs777872624	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1060007	GCTGAGGCAGGAGAA[C/T]CACTTGAACCTGGGA	285498
rs777885956	snp	C/T	3.29457e-05	0.00405854	missense, utr-variant-5-prime, nc-transcript-variant	RNF212	GRCh38.p7	4:1096833	ATGCCTGGATATCTG[C/T]GTCGGTCTGAAAGAG	285498
rs777933273	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1109558	TGAGAGGTGGATTCA[C/G]AGACTTGAGGATTCC	285498
rs777963191	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1069807	AACTGTTGAGGACAA[C/G]AAAAAGAAGTATGAA	285498
rs778012404	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1085080	CTACACACACAGCCA[A/G]TGGGAGGCAGACAGG	285498
rs778099583	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1106545	ACATATTAGAGATTA[C/T]TTAGAAATCAGAGAA	285498
rs778125534	snp	A/T			intron-variant	RNF212	GRCh38.p7	4:1103692	ATAAAATATTTATAG[A/T]CAATAATCACAGAAA	285498
rs778233270	snp	G/T	2.01731e-05	0.00317587	utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant	RNF212, LOC105374344	GRCh38.p7	4:1113495	GCAGCGGCGAGGCCG[G/T]GCCCACGCGAAGCCC	285498
rs778234523	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1064943	CATAGCGTCCTCAAT[A/G]TTCATCCACGCGGTA	285498
rs778240434	snp	A/G	1.72519e-05	0.00293695	missense, upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant	RNF212, LOC105374344	GRCh38.p7	4:1113422	AGCACGACGTCCTGT[A/G]GGGCGGCTGGAAGCA	285498
rs778272318	in-del	-/AAA			intron-variant	RNF212	GRCh38.p7	4:1063697	GAGACTCAGTCTCAA[-/AAA]AAAAAAAAAAAAGAA	285498
rs778282697	in-del	-/A			utr-variant-3-prime, intron-variant	RNF212	GRCh38.p7	4:1071711	AATGAAATGCAAAAT[-/A]AAACAGCAAGATACC	285498
rs778313087	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1077513	GCTGAAGTTATAGGC[A/G]TGAGCCCGACATGCC	285498
rs778339128	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1080914	GCTCCCTGTGCCAGA[A/G]TGATGGCCAGGCAGG	285498
rs778369567	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1107741	AGGCATGAGCCATCA[C/T]GCCCGGCAGGACTTA	285498
rs778404758	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1076495	GAACAGTGTGGGAGG[C/T]TCACCTCGAGAGAGG	285498
rs778425137	snp	C/T	0.000133187	0.00815939	intron-variant	RNF212	GRCh38.p7	4:1090878	GCTGACACAGATCCA[C/T]GGTCTCTGTGGCTGG	285498
rs778428838	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1063196	TTTGTCAGCAGAAAT[A/G]GGAAAGTTGATCCTA	285498
rs778460970	in-del	-/T			intron-variant	RNF212	GRCh38.p7	4:1106323	AAAAGAACACACGCC[-/T]TTTTAAACACCAATC	285498
rs778525089	snp	C/G/T	9.37174e-05	0.00684482	intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1113343	CTCCAGCCTGCGTTC[C/G/T]GGAAGCCCTGACCTT	285498
rs778538960	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1066867	ATATCCAGGAAATCA[C/T]TGCCACATCCAACAT	285498
rs778542114	snp	A/G	1.67528e-05	0.00289415	intron-variant	RNF212	GRCh38.p7	4:1086006	GCTATGCTGAGTGAC[A/G]TGTGACCCTCTAAAT	285498
rs778576502	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1111067	CGTCTCCATCATTCC[C/T]AACAATGTTATCTTC	285498
rs778578623	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1099981	AGCCACTGCCGCTAG[A/G]CAGGAACGGGGTTCT	285498
rs778593121	snp	A/G			intron-variant, missense	RNF212	GRCh38.p7	4:1094326	GGACTGCAGCTGTCC[A/G]GTGACATCCAAGGAG	285498
rs778615956	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1069029	CATGGGCAACATGGC[A/G]AAACTCCATCTCTAC	285498
rs778648460	snp	C/T	5.00413e-05	0.00500181	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1073197	TTAGATGTGGCCCTG[C/T]GGGAAGATGCAGGAG	285498
rs778666511	snp	G/T			intron-variant	RNF212	GRCh38.p7	4:1110180	AGACAAAGGGATTGA[G/T]GCCTGATCTATAAAT	285498
rs778685895	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1089890	CCCAGTCATGCGGAA[A/C]TGTGAGTCCATTCAA	285498
rs778738659	snp	C/G	1.64743e-05	0.00287			GRCh38.p7	4:1073125	TGGAAATGACACACT[C/G]TCCGGGCACAGGGGG	285498
rs778749225	snp	C/T					GRCh38.p7	4:1104433	CTCTGCCCTGTTCTC[C/T]AGGGCTTCTGTGGTG	285498
rs778798617	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1090624	ATAGGCTGCTCAGAA[A/G]GAGACAGTGACAACG	285498
rs778817257	in-del	-/C			intron-variant	RNF212	GRCh38.p7	4:1099677	GGGGTGTGTGCGCCA[-/C]CAATGGTACAGTAAC	285498
rs778931144	snp	A/G	1.64933e-05	0.00287165	synonymous-codon, intron-variant, nc-transcript-variant	RNF212	GRCh38.p7	4:1081436	GTCGGGGGCTGATGA[A/G]TGAGGTGGCAGCAGG	285498
rs778978231	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1099114	ACCTCAGTGAGGCCT[C/G]AGCGGGAGAACACAG	285498
rs779031825	snp	A/G	1.65195e-05	0.00287393	intron-variant	RNF212	GRCh38.p7	4:1081506	CCAGCGTCAGTGCAC[A/G]CAGTGTGACTCAGCA	285498
rs779033191	snp	A/G			upstream-variant-2KB, intron-variant	RNF212, LOC105374344	GRCh38.p7	4:1114546	TAACATGATATTTTT[A/G]ATATATTAGGTTAAA	285498
rs779100940	snp	A/G	0.000288184	0.0120004	intron-variant, missense, downstream-variant-500B	RNF212	GRCh38.p7	4:1093579	CTGAGAGGCACGAGA[A/G]GCAGAGCAGACAGGT	285498
rs779208492	snp	A/G	2.07333e-05	0.00321966	utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant	RNF212, LOC105374344	GRCh38.p7	4:1113502	CGAGGCCGGGCCCAC[A/G]CGAAGCCCACGCAAG	285498
rs779307443	in-del	-/A			downstream-variant-500B, intron-variant	RNF212	GRCh38.p7	4:1071452	TAATGTCAAGAGAAC[-/A]AAGGACAAGCCACAA	285498
rs779349292	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1105839	TAAGGCTGTGGGGGA[C/T]GGAGCCTGTGGCCAT	285498
rs779353807	in-del	-/AAC	0.000116076	0.00761737	intron-variant	RNF212	GRCh38.p7	4:1079738	CCAGGACTTACCTCT[-/AAC]AACGTCAGTTGAAAT	285498
rs779376102	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1057465	GAGAAGAGCAGGGGG[A/C]GGTGAACTGTGGTCT	285498
rs779384704	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1076540	TCTGCAGGCCAGAGA[A/G]TGAGACCTCAGTCTG	285498
rs779407923	snp	C/T	4.96644e-05	0.00498294	intron-variant	RNF212	GRCh38.p7	4:1090851	AATCTGAAAAGATCA[C/T]AGGTTTCAGCTGCTG	285498
rs779439703	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1078122	ACGACTGAGTTCATA[C/T]CTATAAAGGGCTCGG	285498
rs779462579	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1067417	ATAGATTATAATAGA[C/T]CAAAAAAAGATCTAA	285498
rs779483360	snp	A/G	0.000157965	0.00888582	intron-variant, synonymous-codon, downstream-variant-500B	RNF212	GRCh38.p7	4:1093811	GAGGGGGTGAGGTGC[A/G]TCCTGGATGGTGTTT	285498
rs779549423	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1063392	CCTACAGGACAATAC[A/G]ATTAACAGCTGACTT	285498
rs779571020	snp	G/T	3.29826e-05	0.00406082	missense, utr-variant-3-prime, nc-transcript-variant	RNF212	GRCh38.p7	4:1073612	ACCCATTCGTCCATC[G/T]TGAGGTGGACTAATC	285498
rs779593768	snp	A/G	8.23744e-05	0.0064172	synonymous-codon, missense, intron-variant, downstream-variant-500B, nc-transcript-variant	RNF212	GRCh38.p7	4:1073129	AATGACACACTCTCC[A/G]GGCACAGGGGGCTTA	285498
rs779604423	snp	C/T	1.67978e-05	0.00289804	intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1073207	CCCTGCGGGAAGATG[C/T]AGGAGACAGCGTGTG	285498
rs779612755	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1111305	TCTAGGATTATAGGA[C/T]TATTATCCCGTATTA	285498
rs779684181	snp	A/C	3.30715e-05	0.00406628	intron-variant	RNF212	GRCh38.p7	4:1090749	ATCTAAAGGTCAAAA[A/C]AATTCAAGTGGCAAT	285498
rs779712456	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1090011	TGAGGGGTGACAGGA[C/T]GGGATGAGGGGTGAC	285498
rs779810163	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1073893	TGTTTGATTCCCTCT[C/G]TTCCACCAGGGCCTA	285498
rs779850376	snp	A/G			utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	RNF212	GRCh38.p7	4:1056457	GGAGGCATGGAAGTC[A/G]CGGTAAAAACACAAC	285498
rs779858396	snp	C/T	1.65345e-05	0.00287524	missense, utr-variant-5-prime, intron-variant, nc-transcript-variant	RNF212	GRCh38.p7	4:1108347	TTTCAACTTACATGC[C/T]TTGAAAGCAAAACTG	285498
rs779917413	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1081891	ACTCAGCACATGGCC[A/G]CTGCGGGTGTTAAAG	285498
rs779930249	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1067736	GGGTGAGGTGCTGCA[C/T]GCCTGTAATTAATCC	285498
rs780008059	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1104692	CACTCCCCCAGAGTG[A/G]AGCGCCCCCACCACC	285498
rs780016027	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1078598	AGTTTACTACTGTCT[C/T]CTTCAGCACTGTTTG	285498
rs780152837	in-del	-/ACC			intron-variant	RNF212	GRCh38.p7	4:1108836	CCCTGAGTAGCTAGG[-/ACC]ACAGACGTGTGCCGC	285498
rs780250512	snp	C/T	1.73246e-05	0.00294312	utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1072833	ACACAGAGGAATAAA[C/T]TGAAAACACTCAGAA	285498
rs780288611	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1077856	CACCCATAAGGAAGC[A/G]TGTCCCTCTGGAAGC	285498
rs780309091	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1088481	TGGAACTTATGTTTA[A/G]AAGGGAAGCAGAACA	285498
rs780323670	snp	C/T			intron-variant, utr-variant-5-prime	RNF212	GRCh38.p7	4:1099787	ATGGAGGAAATCAAC[C/T]CTGGTGCAGAGCAAT	285498
rs780351099	snp	G/T	0.000156875	0.00885511	intron-variant, missense, downstream-variant-500B	RNF212	GRCh38.p7	4:1093851	TCTGGCTGGCTCTGG[G/T]ACCGCCGGCATCCTG	285498
rs780357873	in-del	-/G			intron-variant	RNF212	GRCh38.p7	4:1062754	CATCGTGGTTGGAAA[-/G]GAAAAAGTAAAACAA	285498
rs780488394	snp	C/T			intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1093287	CTGTTGGTATTTACC[C/T]TATTAGAAATTAAGA	285498
rs780533022	snp	A/G	1.64955e-05	0.00287184	stop-gained, utr-variant-3-prime, nc-transcript-variant	RNF212	GRCh38.p7	4:1073605	TTTACTTACCCATTC[A/G]TCCATCTTGAGGTGG	285498
rs780593001	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1068807	ATTTTAAAATGTTAA[C/T]TTCATTGGATACAGA	285498
rs780643771	snp	C/G/T	3.31182e-05	0.00406918	synonymous-codon, intron-variant, missense, nc-transcript-variant	RNF212	GRCh38.p7	4:1079679	GAGATCAACTTCCAT[C/G/T]GACTCCAGTCTGTTA	285498
rs780719021	snp	A/C	0.000185615	0.00963187	intron-variant, utr-variant-5-prime	RNF212	GRCh38.p7	4:1099843	AGCGGACACGGGTAC[A/C]CCTGTGCGGGATCCA	285498
rs780749877	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1102275	CAGTCATCCTTCAGT[A/C]TATGAGGGTAAATTG	285498
rs780779702	snp	A/G			synonymous-codon, nc-transcript-variant	RNF212	GRCh38.p7	4:1058362	ACTCGTTGTCAGGCC[A/G]GGATGCTCGGGGCCC	285498
rs780806123	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1064930	CTTATGCACTTAGCA[C/T]AGCGTCCTCAATGTT	285498
rs780852482	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1103347	CCCATCTTACAAAAA[A/G]TTTTCCAGAGAAGAG	285498
rs780880376	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1060964	AGAAATCAATGAGTT[A/C]TCTCTACGAAGCCAA	285498
rs780979134	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1061917	CAAAGAAACAGAAGC[A/G]TGACCACACTCAGGG	285498
rs781017805	snp	A/G	1.66774e-05	0.00288763	intron-variant	RNF212	GRCh38.p7	4:1085869	GGGTGCCTCGACTGC[A/G]CACTCACGGGGGGTG	285498
rs781018063	snp	C/T	3.4246e-05	0.00413785	intron-variant	RNF212	GRCh38.p7	4:1081629	CTCATACTAAATAGA[C/T]GGAGAAAAGGTATTG	285498
rs781089621	snp	A/T			intron-variant	RNF212	GRCh38.p7	4:1065192	ATTGTGTTTTTAAGT[A/T]TTGGAGGAAAGGCCA	285498
rs781096315	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1085504	GTACCTTTCGCAAAC[A/G]GCTACGACTCCTGGC	285498
rs781160000	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1069000	ATTGCCTAAGCTCAG[A/G]AGTTTGAGACCATCA	285498
rs781227203	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1108085	TTGTGCTGCAGAAAT[C/T]TATTTAACCCACTTT	285498
rs781248635	snp	A/T			utr-variant-3-prime, intron-variant	RNF212	GRCh38.p7	4:1072000	AATTCATAATTGCCA[A/T]AACTTGGAAGCAACC	285498
rs781307451	snp	C/T	3.25505e-05	0.00403413	missense, utr-variant-3-prime, intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1072891	AAAATGACTTTTTCC[C/T]TTCAAATTGGCAAAG	285498
rs781343456	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1076307	GGAAAAGAACCAATC[C/G]CCTCTGGGCGGGCCC	285498
rs781369392	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1080113	CACACATACCACACC[A/G]TGCACGCTCGGTACG	285498
rs781431533	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1085840	AGAGCCAGACGACCA[A/G]TGCACATGGCAGTGG	285498
rs781465457	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1064383	GAAATAATAAAGCAC[A/C]CAGATAAAGTATCAA	285498
rs781502373	snp	C/T	4.94882e-05	0.0049741	missense, intron-variant, nc-transcript-variant	RNF212	GRCh38.p7	4:1081423	AACCCACACACCTGT[C/T]GGGGGCTGATGAGTG	285498
rs781524953	snp	G/T			intron-variant, upstream-variant-2KB	RNF212, LOC105374344	GRCh38.p7	4:1112272	ACAGAAAGCGGCTTT[G/T]CTGTAGGGCTGGTTG	285498
rs781528258	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1105432	AATCGTAATGGAGCA[C/T]TATAATGACAAACAA	285498
rs781542530	in-del	-/C	1.6473e-05	0.00286988	frameshift-variant, intron-variant, nc-transcript-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1073083	GCCAGTGAGGACAGA[-/C]GTCTATGCAGAAACA	285498
rs781550525	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1099686	TGCGCCACAATGGTA[C/G]AGTAACGAGGATACA	285498
rs781632969	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1111316	AGGATTATTATCCCG[C/T]ATTAATCGCTCCCCA	285498
rs781636719	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1075443	AGGGGGAGCAGGCGC[A/G]TTGCAGGGCGAGCAG	285498
rs796090107	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1109582	GGATTCCAACGCTGC[C/T]GAGTCAGCAACACTG	285498
rs796116435	in-del	-/A			intron-variant	RNF212	GRCh38.p7	4:1102594	AAAACACAAAAAAAC[-/A]AAAAAAAAAACACTT	285498
rs796167456	in-del	-/AT			intron-variant	RNF212	GRCh38.p7	4:1083945	TTCCACATTTTGTGC[-/AT]TTTTTTTTTTTTTTT	285498
rs796188951	snp	A/G			downstream-variant-500B	RNF212	GRCh38.p7	4:1056079	GGATGTGGCGGCGCC[A/G]ACCCACGCTGCGTGC	285498
rs796215488	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1059153	CTGCTGCGGCACGTC[A/G]GGGGGTTGCCGGCTT	285498
rs796227114	in-del	-/AC			intron-variant, frameshift-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1093540	TGGGCAGAGCCTGTG[-/AC]CTCCACGGCCCATGC	285498
rs796269585	snp	A/C			intron-variant	RNF212	GRCh38.p7	4:1102987	CTCTACTAAAAAAAT[A/C]CAAAAAAAAAAAAAA	285498
rs796284494	in-del	-/ACACACACACACACACAC			intron-variant	RNF212	GRCh38.p7	4:1106250	TAAACAATTTTACTT[-/ACACACACACACACACAC]ACACACACACACACA	285498
rs796288588	multinucleotide-polymorphism	CA/TG			intron-variant	RNF212	GRCh38.p7	4:1090349	CTGGCTTCCAGACTT[CA/TG]GGAAGCGGCCCCAGG	285498
rs796289259	multinucleotide-polymorphism	CA/TG			intron-variant	RNF212	GRCh38.p7	4:1074989	GTCCCTTCGAACTAC[CA/TG]TCCATTTGCTGCTCC	285498
rs796313832	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1070020	AGCGTGGACGCCTGG[C/T]CTGAGTTACAGGTGG	285498
rs796315657	in-del	-/TT			intron-variant	RNF212	GRCh38.p7	4:1064586	TTCATACGGCCTCTT[-/TT]GTGTGTGTGCAGAGT	285498
rs796350278	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1097759	TAGGCATGGAGCTGC[C/T]GTGAGCTAGAATCGC	285498
rs796361989	in-del	-/AAAA			intron-variant	RNF212	GRCh38.p7	4:1063708	TCAAAAAAAAAAAAA[-/AAAA]GAAAAAAGAAAAATT	285498
rs796425712	in-del	-/AA			intron-variant, downstream-variant-500B	RNF212	GRCh38.p7	4:1058062	AGTGAGACTCCGGCT[-/AA]AAAAAAAAAAAGCAA	285498
rs796482168	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1078835	ACACAGGACCAACAC[A/G]GGACCAACACAGGAC	285498
rs796509259	snp	C/T			downstream-variant-500B	RNF212	GRCh38.p7	4:1055797	ACTAACCCCATAAGC[C/T]TCTTTTCCAACCCTG	285498
rs796514344	in-del	AC/CTGCCCAGGCTGGAGCCAGCCAT			intron-variant, cds-indel, downstream-variant-500B	RNF212	GRCh38.p7	4:1093540	GGGCAGAGCCTGTGA[AC/CTGCCCAGGCTGGAGCCAGCCAT]TCCACGGCCCATGCC	285498
rs796564427	multinucleotide-polymorphism	CC/TT			intron-variant	RNF212	GRCh38.p7	4:1102476	ACACACAGTTAAAAC[CC/TT]GTGTTGTTCAAGAGT	285498
rs796668859	snp	A/G			intron-variant	RNF212	GRCh38.p7	4:1102247	CAGAGCTAAAAATTA[A/G]TTTTTGAAAATACAG	285498
rs796670525	in-del	AAAA/T			intron-variant	RNF212	GRCh38.p7	4:1102996	AAAATACAAAAAAAA[AAAA/T]AATCACTAACATTTG	285498
rs796708596	snp	C/T			upstream-variant-2KB, intron-variant, utr-variant-5-prime	RNF212, LOC105374344	GRCh38.p7	4:1113758	CGGTCCTCAGGTGTT[C/T]TGTGGAAGCCGGGCC	285498
rs796734465	in-del	-/ATTACCTG			intron-variant	RNF212	GRCh38.p7	4:1073864	GTGGTGTGGGTGGGT[-/ATTACCTG]ATTACCTGTTTGATT	285498
rs796735265	snp	C/T			intron-variant	RNF212	GRCh38.p7	4:1107966	AGGCATTGTTTTAAG[C/T]CTGCAGCAGTAATTG	285498
rs796754892	multinucleotide-polymorphism	AC/GT			intron-variant	RNF212	GRCh38.p7	4:1078827	AGGGTCAACACAGGA[AC/GT]AACACGGGACCAACA	285498
rs796772526	snp	G/T			intron-variant	RNF212	GRCh38.p7	4:1088280	AGGTCACTCTTGCTG[G/T]GCTTTAGCAAAGAGA	285498
rs796809058	snp	A/T			intron-variant	RNF212	GRCh38.p7	4:1082287	CCACCTGCTGTGCCC[A/T]GTGACTCCCGGCCAC	285498
rs796867763	snp	C/G			intron-variant	RNF212	GRCh38.p7	4:1064334	TCACTGTGGTGAGTT[C/G]AAGATGCATGTTGTA	285498
rs796884947	in-del	-/AG			intron-variant	RNF212	GRCh38.p7	4:1064968	GCGGTAGCGTGTGCC[-/AG]AGTTTCCTTCCATTT	285498
rs796909857	in-del	-/AAA			intron-variant	RNF212	GRCh38.p7	4:1063695	GTGAGACTCAGTCTC[-/AAA]AAAAAAAAAAAAAAG	285498
rs796931180	in-del	-/TG			intron-variant	RNF212	GRCh38.p7	4:1070051	TTCGTAGGACTATGC[-/TG]TGTCAGCGTGGACGC	285498
rs796955315	snp	G/T			intron-variant	RNF212	GRCh38.p7	4:1081225	CTCTGATTGGCCACC[G/T]GGATCACACACTTAG	285498

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